COMPREHENSIVE SRS INSTRUMENT
- Primary DI
- 00880304542037
- Brand
- COMPREHENSIVE SRS INSTRUMENT
- Company
- Biomet Orthopedics, LLC
- Model
- 405118
- Catalog number
- 405118
- Published
- 2016-10-27
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JDC | Prosthesis, Elbow, Constrained, Cemented | Orthopedic | 2 |
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| MBF | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K111746 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304542037 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304542037 | 00880304542037 | 880304542037 | 0880304542037 |
GMDN Terms#
| Term | Definition |
|---|---|
| Humeral stem prosthesis trial | A copy of a final humeral stem prosthesis 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 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 |
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- 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 |
|---|---|---|---|---|
| 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 |
| 00880304434363 | Vanguard® Knee System | 184270 | 184270 | 2015-10-24 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| B1132A2HI000100 | Shoulder Innovations InSet 95 Humeral Stem | Shoulder Innovations, Inc. | KWT | 2026-05-28 |
| B1132A2HI000100 | Shoulder Innovations InSet 95 Humeral Stem | Shoulder Innovations, Inc. | MBF | 2026-05-28 |
| B1132A2HI000100 | Shoulder Innovations InSet 95 Humeral Stem | Shoulder Innovations, Inc. | KWS | 2026-05-28 |
| 08033390002233 | SMR System | LIMACORPORATE SPA | MBF | 2026-02-19 |
| 08033390002240 | SMR System | LIMACORPORATE SPA | MBF | 2026-02-19 |
| 08033390002257 | SMR System | LIMACORPORATE SPA | MBF | 2026-02-19 |
| 07613327668889 | Modular Elbow | Howmedica Osteonics Corp. | JDC | 2025-02-24 |
| 07613327668902 | Modular Elbow | Howmedica Osteonics Corp. | JDC | 2025-02-24 |
| 07613327668919 | Modular Elbow | Howmedica Osteonics Corp. | JDC | 2025-02-24 |
| 07613327603361 | REUNION | Stryker GmbH | KWS | 2024-10-01 |
| 07613327354331 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327354355 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327354805 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327354904 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327354935 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327354942 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355024 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355093 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355109 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355222 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355246 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355260 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355291 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355345 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355369 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355437 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355444 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327355475 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
| 07613327590050 | Axel Pin Assembly Standard Elbow | Howmedica Osteonics Corp. | JDC | 2022-03-23 |
| 07613327590074 | Bearing and Axle Bushing Assembly - Standard Elbow | Howmedica Osteonics Corp. | JDC | 2022-03-23 |