MEDICAL DEVICES AND SUPPLIES Sample Clauses

MEDICAL DEVICES AND SUPPLIES. CareFirst BlueChoice provides benefits for Medical Devices and Supplies obtained through designated Contracting Providers.
Sample 1Sample 2Sample 3See All (11)
AutoNDA by SimpleDocs
MEDICAL DEVICES AND SUPPLIES. See the Prior Authorization Amendment for Covered Services that may require prior authorization.
Sample 1Sample 2Sample 3See All (4)
MEDICAL DEVICES AND SUPPLIES. See the Prior Authorization Amendment for Covered Services that may require prior authorization. CareFirst BlueChoice provides benefits for Medical Devices and Supplies obtained through designated Contracting Providers.
Sample 1Sample 2Sample 3
MEDICAL DEVICES AND SUPPLIES. Benefits will not be provided for purchase, rental, or repair of the following:
Sample 1Sample 2
MEDICAL DEVICES AND SUPPLIES. Medical Devices and Supplies No annual dollar limit 90% of the Allowed Benefit In-Network and Out-of-Network Deductibles apply 70% of the Allowed Benefit Hair Prosthesis Limited to maximum payment of $350 per Benefit Period Benefit does not apply to any annual maximums for Medical Devices and Supplies 100% of the Allowed Benefit No 100% of the Allowed Benefit Group Hospitalization and Medical Services, Inc. doing business as CareFirst BlueCross BlueShield (CareFirst) 000 Xxxxx Xxxxxx, XX Xxxxxxxxxx, XX 20065 000-000-0000 An independent licensee of the Blue Cross and Blue Shield Association INTER-PLAN ARRANGEMENTS DISCLOSURE AMENDMENT This amendment is effective on the effective date of the Evidence of Coverage to which this amendment is attached.
Sample 1
MEDICAL DEVICES AND SUPPLIES. Medical Devices and Supplies No annual dollar limit 90% of the Allowed Benefit In-Network and Out-of-Network Deductibles apply 70% of the Allowed Benefit Hair Prosthesis Limited to maximum payment of $350 per Benefit Period Benefit does not apply to any annual maximums for Medical Devices and Supplies 100% of the Allowed Benefit No 100% of the Allowed Benefit Group Hospitalization and Medical Services, Inc. doing business as CareFirst BlueCross BlueShield (CareFirst) 000 Xxxxx Xxxxxx, XX Xxxxxxxxxx, XX 20065 000-000-0000 An independent licensee of the Blue Cross and Blue Shield Association INTER-PLAN ARRANGEMENTS DISCLOSURE AMENDMENT This amendment is effective on the effective date of the Evidence of Coverage to which this amendment is attached. Out-of-Area Services Overview CareFirst has a variety of relationships with other Blue Cross and/or Blue Shield Licensees. Generally, these relationships are called “Inter-Plan Arrangements.” These Inter-Plan Arrangements work based on rules and procedures issued by the Blue Cross Blue Shield Association (“Association”). Whenever you access healthcare services outside the geographic area CareFirst serves, the claim for those services may be processed through one of these Inter-Plan Arrangements. The Inter-Plan Arrangements are described below. When you receive care outside of CareFirst service area, you will receive it from one of two kinds of providers. Most providers (“participating/PPO providers”) contract with the local Blue Cross and/or Blue Shield Plan in that geographic area (“Host Blue”). Some providers (“non-participating providers”) don’t contract with the Host Blue. CareFirst explains below how we pay both kinds of providers.
Sample 1
MEDICAL DEVICES AND SUPPLIES. The P.A. shall be responsible for providing all treatment devices and medical supplies necessary for the performance of its services required to be performed by it or its employees under the terms of this Agreement. All sales taxes incurred in connection with acquiring such equipment and supplies shall be borne by the PA.
Sample 1
AutoNDA by SimpleDocs

Related to MEDICAL DEVICES AND SUPPLIES

  • Manufacturing and Supply Genentech shall be responsible for manufacturing and supplying Licensed Products for clinical use and commercial sale in the Genentech Field.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time.

  • Manufacturing Services Jabil will manufacture the Product in accordance with the Specifications and any applicable Build Schedules. Jabil will reply to each proposed Build Schedule that is submitted in accordance with the terms of this Agreement by notifying Company of its acceptance or rejection within three (3) business days of receipt of any proposed Build Schedule. In the event of Jabil’s rejection of a proposed Build Schedule, Jabil’s notice of rejection will specify the basis for such rejection. When requested by Company, and subject to appropriate fee and cost adjustments, Jabil will provide Additional Services for existing or future Product manufactured by Jabil. Company shall be solely responsible for the sufficiency and adequacy of the Specifications [***].

  • Products and Services General Information The Vendor Agreement (“Agreement”) made and entered into by and between The Interlocal Purchasing System (hereinafter “TIPS”) a government cooperative purchasing program authorized by the Region 8 Education Service Center, having its principal place of business at 0000 XX Xxx 000 Xxxxx, Xxxxxxxxx, Xxxxx 00000 and the TIPS Vendor. This Agreement consists of the provisions set forth below, including provisions of all attachments referenced herein. In the event of a conflict between the provisions set forth below and those contained in any attachment, the provisions set forth shall control unless otherwise agreed by the parties in writing and by signature and date on the attachment. A Purchase Order (“PO”), Agreement or Contract is the TIPS Member’s approval providing the authority to proceed with the negotiated delivery order under the Agreement. Special terms and conditions as agreed between the Vendor and TIPS Member should be added as addendums to the Purchase Order, Agreement or Contract. Items such as certificate of insurance, bonding requirements, small or disadvantaged business goals are some, but not all, of the possible addendums.

  • Products Products available under this Contract are limited to Software, including Software as a Service, products and related products as specified in Appendix C, Pricing Index. Vendor may incorporate changes to their product offering; however, any changes must be within the scope of products awarded based on the posting described in Section 1.B above. Vendor may not add a manufacturer’s product line which was not included in the Vendor’s response to the solicitation described in Section 1.B above.

  • Manufacture of Products All Products marketed through Grantor's Web ------------------------- Site shall be manufactured, packaged, prepared, and shipped in accordance with the specifications and requirements described on Exhibit A hereto as it may be modified from time to time. Quality control standards relating to the Product's weight, color, consistency, micro-biological content, labeling and packaging are also set forth on Exhibit A. In the event that Exhibit A is incomplete, Products shall be manufactured and shipped in accordance with industry standards.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements.

  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

  • Manufacture of Product Prior to commercialization of the Product, the Parties may, if appropriate for both parties, negotiate in good faith a manufacturing and supply agreement to provide for Licensor to fulfill the manufacturing requirements of Licensee for Product for sale in the European market. The cost of such manufacturing shall not be greater than * percent (*%) of the cost of any competitor cGMP contract manufacturing facility that proposes to manufacturer the Product for Licensee. * Confidential information has been omitted and filed confidentially with the Securities and Exchange Commission.

  • Manufacture and Supply Subject to the terms and conditions of this Agreement, Collaboration Products shall be manufactured and supplied for preclinical and clinical testing and for commercial sale upon the following terms and conditions:

Time is Money Join Law Insider Premium to draft better contracts faster.