Arthrex®
- Primary DI
- 00888867020498
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-1648
- Catalog number
- AR-1648
- Device description
- TRIMANO DRAPE
- Published
- 2018-08-03
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| PUI | Drape, surgical, exempt |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| PUI | Drape, Surgical, Exempt | General, Plastic Surgery | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10888867020495 | Package | GS1 | 10 | In Commercial Distribution |
| 00888867020498 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10888867020495 | 10888867020495 | ||
| 00888867020498 | 00888867020498 | 888867020498 | 0888867020498 |
GMDN Terms#
| Term | Definition |
|---|---|
| Medical equipment/instrument drape, single-use | A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device. |
Contacts#
| Phone | |
|---|---|
| +1(800)934-4404 | complaints@arthrex.com |
Regulatory Flags#
- DUNS number
- 131747628
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888867620964 | Arthrex® | AR-3210-0067 | AR-3210-0067 | 2026-10-12 |
| 00888867620971 | Arthrex® | AR-3210-0067-PK | AR-3210-0067-PK | 2026-10-12 |
| 00888867620988 | Arthrex® | AR-3210-0068 | AR-3210-0068 | 2026-10-12 |
| 00888867620995 | Arthrex® | AR-3210-0068-PK | AR-3210-0068-PK | 2026-10-12 |
| 00888867520745 | Arthrex® | AR-1360FT-KFT | AR-1360FT-KFT | 2026-01-21 |
| 00888867429857 | Arthrex® | AR-2600FSB-1 | AR-2600FSB-1 | 2023-05-24 |
| 00888867429864 | Arthrex® | AR-2600FSB-2 | AR-2600FSB-2 | 2023-05-24 |
| 00888867429871 | Arthrex® | AR-2600FSB-3 | AR-2600FSB-3 | 2023-05-24 |
| 00888867429888 | Arthrex® | AR-2600FSB-4 | AR-2600FSB-4 | 2023-05-24 |
| 00888867354067 | Arthrex® | AR-1360FT-BC | AR-1360FT-BC | 2020-12-15 |
| 00888867101951 | Arthrex® | AR-3600DC | AR-3600DC | 2018-12-21 |
| 00888867096066 | Arthrex® | AR-1677BC-CP | AR-1677BC-CP | 2017-02-15 |
| 00888867084384 | Arthrex® | ABS-3005 | ABS-3005 | 2017-02-15 |
| 00888867084407 | Arthrex® | ABS-3008 | ABS-3008 | 2017-02-15 |
| 00888867084421 | Arthrex® | ABS-3016 | ABS-3016 | 2017-02-15 |
| 00888867084148 | Arthrex® | ABS-2001-01 | ABS-2001-01 | 2017-02-15 |
| 00888867084155 | Arthrex® | ABS-2001-02 | ABS-2001-02 | 2017-02-15 |
| 00888867084162 | Arthrex® | ABS-2001-05 | ABS-2001-05 | 2017-02-15 |
| 00888867084179 | Arthrex® | ABS-2001-10 | ABS-2001-10 | 2017-02-15 |
| 00888867084186 | Arthrex® | ABS-2002-01 | ABS-2002-01 | 2017-02-15 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00748426264568 | Medline-Microtek | Microtek Medical LLC | PUI | 2026-10-12 |
| 16931918199627 | Alleset | GRI Medical & Electronic Technology Co., Ltd. | PUI | 2026-09-29 |
| 10809160538999 | Halyard | MEDICAL ACTION INDUSTRIES INC. | PUI | 2026-09-24 |
| 10850091824002 | AeroKEE | Healkee Medical USA Inc. | PUI | 2026-09-24 |
| 10850091824019 | AeroKEE | Healkee Medical USA Inc. | PUI | 2026-09-24 |
| 10197344220083 | MEDLINE | MEDLINE INDUSTRIES, INC. | PUI | 2026-09-18 |
| 10197344220090 | MEDLINE | MEDLINE INDUSTRIES, INC. | PUI | 2026-09-18 |
| 00197998192814 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998304996 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305016 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305030 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305078 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305092 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305115 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305139 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998305153 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312373 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312397 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312434 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312458 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312472 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998312496 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329678 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329708 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329739 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329760 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329791 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329821 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998329852 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |
| 00197998330032 | Solventum™ Steri-Drape™ | Solventum US LLC | PUI | 2026-08-23 |