HOFFMANN
- Primary DI
- 04546540492593
- Brand
- HOFFMANN
- Company
- Stryker GmbH
- Model
- 4921-1-100
- Catalog number
- 4921-1-100
- Device description
- Tube to Rod Coupling 20mm,8mm
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Product Codes#
Code, Name table| Code | Name |
|---|
| JEC | COMPONENT, TRACTION, INVASIVE |
| KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
| LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
Product Code Classifications#
Code, Device, Specialty table| Code | Device | Specialty | Class |
|---|
| JEC | Component, Traction, Invasive | Orthopedic | 2 |
| KTT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component | Orthopedic | 2 |
| LXT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite | Orthopedic | 2 |
Identifiers And Packaging#
Identifier, Type, Agency table| Identifier | Type | Agency | Package quantity | Status |
|---|
| 04546540492593 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
Source identifier, GTIN-14 normalized, EAN-13 table| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 04546540492593 | 04546540492593 | 4546540492593 |
Sterilization Methods#
Method table| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 481999654
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
Other Devices Sharing Product Codes#
Primary DI, Brand, Company table| Primary DI | Brand | Company | Product code | Published |
|---|
| 07613327616859 | HOFFMANN LRF | Stryker GmbH | KTT | 2026-07-23 |
| 07613327616880 | HOFFMANN LRF | Stryker GmbH | KTT | 2026-07-23 |
| 07613327616835 | HOFFMANN LRF | Stryker GmbH | KTT | 2026-07-21 |
| 07613327616866 | HOFFMANN LRF | Stryker GmbH | KTT | 2026-07-21 |
| 10888867544571 | Arthrex® | ARTHREX, INC. | KTT | 2026-03-13 |
| 00810028396166 | EF1 | Medshape, Inc. | KTT | 2024-07-09 |
| 00810028396340 | EF1 | Medshape, Inc. | KTT | 2024-07-09 |
| 00810028396333 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396357 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396371 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396159 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396173 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396142 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396364 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00810028396388 | EF1 | Medshape, Inc. | KTT | 2024-05-31 |
| 00885556819791 | UNI-CP Compression Plate | Smith & Nephew, Inc. | LXT | 2023-10-26 |
| 00885556839942 | Total Wrist Fusion System | Smith & Nephew, Inc. | LXT | 2022-12-21 |
| 00885556839959 | Total Wrist Fusion System | Smith & Nephew, Inc. | LXT | 2022-12-21 |
| 00885556839966 | Total Wrist Fusion System | Smith & Nephew, Inc. | LXT | 2022-12-21 |
| 00887868549236 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549243 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549250 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549267 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549274 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549281 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549298 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549304 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549311 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549328 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |
| 00887868549335 | MULTI-DIRECTIONAL SCREW | Biomet Orthopedics, LLC | LXT | 2022-11-14 |