PRIMA
- Primary DI
- 08033390215749
- Brand
- PRIMA
- Company
- LIMACORPORATE SPA
- Model
- 9013.67.336
- Catalog number
- 9013.67.336
- Device description
- PRIMA - Trial Tray #M - Insert #M RET 7° 42 - +6mm
- Published
- 2022-03-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| LHX | Trousers, Anti-Shock |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| LHX | Trousers, Anti-Shock | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 08033390215749 | Primary | GS1 | 0 | |
Alternate GTIN/UPC/EAN values are derived from GS1 digit structure for lookup convenience. Do not treat derived UPC-A or EAN-13 values as separate FDA identifiers. GTIN-14 values with indicator digits 1-9 usually represent packaging levels, cases, pallets, or variable-measure items and are not converted to UPC-A/EAN-13 here.
Alternate GTIN / UPC / EAN Codes
| Source identifier | Source length | GTIN-14 normalized | Indicator | EAN-13 | Conversion note |
|---|
| 08033390215749 | 14 | 08033390215749 | 0 | 8033390215749 | Indicator 0 allows EAN-13 conversion; UPC-A requires prefix 00. |
GMDN Terms
| Term | Definition |
|---|
| Reverse shoulder cup prosthesis trial | A copy of a final reverse shoulder prosthesis cup designed to be used before primary or revision implant surgery to validate the proper size of the permanent prosthesis required by the patient and to ensure its proper orientation and positioning. It connects to a reverse shoulder prosthesis body and articulates with a reverse shoulder prosthesis head and is typically made of metal and/or polymer. This is a reusable device intended to be sterilized prior to use. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 432066322
- 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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company
Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|
| 00198506089589 | ELMED INCORPORATED | ELMED INCORPORATED | LHX | 2026-03-13 |
| 00198506089596 | ELMED INCORPORATED | ELMED INCORPORATED | LHX | 2026-03-13 |
| 00885556919620 | R3 | Smith & Nephew, Inc. | LHX | 2024-11-06 |
| 00885556919613 | R3 | Smith & Nephew, Inc. | LHX | 2024-11-04 |
| 00191083047300 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047317 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047324 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047331 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047348 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047355 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047362 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00191083047379 | AlloWedge | Rti Surgical, Inc. | LHX | 2024-10-14 |
| 00840343722876 | GEN2 | SURGIX MEDICAL LLC | LHX | 2024-06-28 |
| 08800017205267 | LOSPA Knee System, EXULT Knee System | Corentec Co., Ltd | LHX | 2024-01-12 |
| 08800068981486 | LOSPA Knee System, EXULT Knee System | Corentec Co., Ltd | LHX | 2024-01-12 |
| 00840343720537 | GEN2 | SURGIX MEDICAL LLC | LHX | 2023-12-15 |
| 00840343720957 | GEN2 | SURGIX MEDICAL LLC | LHX | 2023-12-15 |
| 10889981321390 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-12-06 |
| 00840343719326 | Gen2 | SURGIX MEDICAL LLC | LHX | 2023-11-14 |
| 00840343719364 | Gen2 | SURGIX MEDICAL LLC | LHX | 2023-11-14 |
| 00885556910757 | Legion | Smith & Nephew, Inc. | LHX | 2023-09-06 |
| 00840019967655 | Reform® Ti CT Modular MIS Pedicle Screw System | PRECISION SPINE, INC. | LHX | 2023-08-07 |
| 00885556832417 | Salto Talaris Total Ankle Prosthesis | Smith & Nephew, Inc. | LHX | 2023-08-02 |
| 10889981308315 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 10889981308322 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 10889981308339 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 10889981308346 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 10889981308353 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 10889981308438 | Specials | SEASPINE ORTHOPEDICS CORPORATION | LHX | 2023-03-24 |
| 00850005827337 | GENESIS AWL/TAPPER | Genesis Biologics, Inc. | LHX | 2023-03-16 |