Arthrex®
- Primary DI
- 00888867245051
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-1650-02
- Catalog number
- AR-1650-02
- Device description
- Arm Sleeve Connector, S3
- Published
- 2019-05-31
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FMP | Protector, skin pressure |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FMP | Protector, Skin Pressure | General Hospital | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888867245051 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888867245051 | 00888867245051 | 888867245051 | 0888867245051 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic surgical distractor, external | A hand-operated surgical instrument designed to noninvasively distract (force apart) a joint to facilitate an orthopaedic surgical procedure (e.g., hip arthroscopy). It is a mechanical tool with a manual trigger, for distraction and release, intended to be stabilized against a fixation point adjacent to the target joint (e.g., between the knee and the thigh for knee distraction, or between the joint and a patient positioner attached to the operating table). This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)934-4404 | complaints@arthrex.com |
Regulatory Flags#
- DUNS number
- 131747628
- Device count
- 1
- Premarket exempt
- true
- Serial number
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888867007482 | Arthrex® | AR-13100-05.0S | AR-13100-05.0S | 2017-01-20 |
| 00888867007529 | Arthrex® | AR-13100-09.0S | AR-13100-09.0S | 2017-01-20 |
| 00888867007567 | Arthrex® | AR-13100-11.0S | AR-13100-11.0S | 2017-01-20 |
| 00888867007604 | Arthrex® | AR-13100-15.0S | AR-13100-15.0S | 2017-01-20 |
| 00888867007628 | Arthrex® | AR-13100-17.5S | AR-13100-17.5S | 2017-01-20 |
| 00888867008564 | Arthrex® | AR-13200-03.0S | AR-13200-03.0S | 2017-01-20 |
| 00888867204041 | Arthrex® | AR-8952XLS | AR-8952XLS | 2017-07-18 |
| 00888867210424 | Arthrex® | AR-8933L-26S | AR-8933L-26S | 2017-08-31 |
| 00888867210431 | Arthrex® | AR-8933L-28S | AR-8933L-28S | 2017-08-31 |
| 00888867210448 | Arthrex® | AR-8933L-30S | AR-8933L-30S | 2017-08-31 |
| 00888867210462 | Arthrex® | AR-8933L-34S | AR-8933L-34S | 2017-08-31 |
| 00888867210479 | Arthrex® | AR-8933L-36S | AR-8933L-36S | 2017-08-31 |
| 00888867210493 | Arthrex® | AR-8933L-40S | AR-8933L-40S | 2017-08-31 |
| 00888867251960 | Arthrex® | AR-8958-01S | AR-8958-01S | 2017-11-28 |
| 00888867266872 | Arthrex® | AR-8952PPL | AR-8952PPL | 2017-03-28 |
| 00888867266896 | Arthrex® | AR-8952PSR | AR-8952PSR | 2017-03-28 |
| 00888867266957 | Arthrex® | AR-8952PPR | AR-8952PPR | 2017-03-28 |
| 00888867371828 | Arthrex® | AR-8924S | AR-8924S | 2023-05-25 |
| 00888867251939 | Arthrex® | AR-8958-02 | AR-8958-02 | 2017-02-15 |
| 00888867279285 | Arthrex® | AR-7249-12-1 | AR-7249-12-1 | 2017-12-01 |
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| 05056279308458 | Repose Flex Large x10 &Pump x10 | Frontier Therapeutics Inc | FMP | 2026-06-05 |
| 00860010482674 | Acanthus | Acanthus Medical Creations LLC | FMP | 2026-05-27 |
| 10603354600666 | TruVue | EHOB INC | FMP | 2025-03-20 |
| 10603354300696 | WAFFLE | EHOB INC | FMP | 2024-12-18 |
| 07613327632873 | Sage TAP LC | SAGE PRODUCTS, LLC | FMP | 2024-03-26 |
| G096R929220 | 9Line | Rising Eagle Medical LLC | FMP | 2024-01-30 |
| 20845854082536 | Paradigm Revolution | Conmed Corporation | FMP | 2023-06-13 |
| 20845854082901 | Paradigm Revolution | Conmed Corporation | FMP | 2023-06-13 |
| 20845854082918 | Paradigm Revolution | Conmed Corporation | FMP | 2023-06-13 |
| 00609271009004 | DARCO® Body Armor® Toe Guard | DARCO INTERNATIONAL, INC. | FMP | 2023-02-08 |
| 00609271009011 | DARCO® Body Armor® Toe Guard | DARCO INTERNATIONAL, INC. | FMP | 2023-02-08 |
| 00609271009103 | DARCO® Body Armor® Toe Guard | DARCO INTERNATIONAL, INC. | FMP | 2023-02-08 |
| 00609271009110 | DARCO® Body Armor® Toe Guard | DARCO INTERNATIONAL, INC. | FMP | 2023-02-08 |
| 00609271166004 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166011 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166028 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166035 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166042 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166059 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166066 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166073 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166080 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166097 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166103 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166110 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166127 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |
| 00609271166134 | DARCO® PegContour™ Insole | Darco (Europe) GmbH | FMP | 2023-02-08 |