BIO-MODULAR REVERSE INSTRUMENTS
- Primary DI
- 00880304561069
- Brand
- BIO-MODULAR REVERSE INSTRUMENTS
- Company
- Biomet Orthopedics, LLC
- Model
- 405656
- Catalog number
- 405656
- Published
- 2017-07-28
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HWT | TEMPLATE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HWT | Template | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304561069 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304561069 | 00880304561069 | 880304561069 | 0880304561069 |
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. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00889024707726 | SolidLok® | 2810-01-021 | 281001021 | 2026-06-10 |
| 00887868561368 | VersaNail® | 2810-13-037 | 281013037 | 2023-09-07 |
| 00889024707061 | A.L.P.S.® | 2142-35-007 | 214235007 | 2026-05-11 |
| 00889024707078 | DRILL BIT | 231200201 | 231200201 | 2026-05-11 |
| 00889024707085 | DRILL BIT | 8290-29-070 | 829029070 | 2026-05-11 |
| 00880304410541 | FIBER OPTICS FOR RC RETRACTOR | 908534 | 908534 | 2019-06-11 |
| 00880304321946 | BIFURCATED FIBER OPTIC CABLE | 31-555502 | 31-555502 | 2017-07-28 |
| 00880304463912 | 4MM X 9FT. LIGHT CABLE | 906117 | 906117 | 2017-07-28 |
| 00889024707054 | CALIBRATED DRILL BIT | 2142-27-070 | 214227070 | 2026-04-27 |
| 00880304233102 | Biomet® Knee System | 141872 | 141872 | 2015-10-24 |
| 00880304233126 | Biomet® Knee System | 141874 | 141874 | 2015-10-24 |
| 00880304233140 | Biomet® Knee System | 141876 | 141876 | 2015-10-24 |
| 00880304233164 | Biomet® Knee System | 141878 | 141878 | 2015-10-24 |
| 00880304233171 | Biomet® Knee System | 141880 | 141880 | 2015-10-24 |
| 00880304233188 | Biomet® Knee System | 141882 | 141882 | 2015-10-24 |
| 00880304433403 | Vanguard® Knee System | 184144 | 184144 | 2015-10-24 |
| 00880304433410 | Vanguard® Knee System | 184181 | 184181 | 2015-10-24 |
| 00880304433564 | Vanguard® Knee System | 184285 | 184285 | 2015-10-24 |
| 00880304433984 | Vanguard® Knee System | 184280 | 184280 | 2015-10-24 |
| 00880304434356 | Vanguard® Knee System | 184265 | 184265 | 2015-10-24 |
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