Comprehensive® SRS Instrument
- Primary DI
- 00887868504372
- Brand
- Comprehensive® SRS Instrument
- Company
- Biomet Orthopedics, LLC
- Model
- 405233
- Catalog number
- 405233
- Published
- 2022-04-23
- 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 |
|---|---|---|---|---|
| 00887868504372 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887868504372 | 00887868504372 | 887868504372 | 0887868504372 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
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
- Sterilization required before use
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00880304474185 | Arcos® Modular Revision Hip System | 11-302102 | 11-302102 | 2015-10-24 |
| 00880304474246 | Arcos® Modular Revision Hip System | 11-302101 | 11-302101 | 2015-10-24 |
| 00880304539259 | Arcos® Modular Revision Hip System | 11-302109 | 11-302109 | 2015-10-24 |
| 00889024711280 | Jgrknt Reusable Fishmouth Perc Guide | SSI008662 | SSI008662 | 2026-08-25 |
| 00889024712034 | Percutaneous Soft Anchor Short 1.4mm Guide | SSI008661 | SSI008661 | 2026-08-25 |
| 00880304527386 | Active Articulation | 010000990 | 010000990 | 2020-05-15 |
| 00880304527393 | Active Articulation | 010000991 | 010000991 | 2020-05-15 |
| 00880304485020 | Active Articulation Hip System | EP-200144 | EP-200144 | 2015-11-03 |
| 00880304485037 | Active Articulation Hip System | EP-200146 | EP-200146 | 2015-11-03 |
| 00880304485044 | Active Articulation Hip System | EP-200148 | EP-200148 | 2015-10-24 |
| 00880304485051 | Active Articulation Hip System | EP-200150 | EP-200150 | 2015-10-24 |
| 00880304485068 | Active Articulation Hip System | EP-200152 | EP-200152 | 2015-10-24 |
| 00880304485075 | Active Articulation Hip System | EP-200154 | EP-200154 | 2015-10-24 |
| 00880304485082 | Active Articulation Hip System | EP-200156 | EP-200156 | 2015-10-24 |
| 00880304485099 | Active Articulation Hip System | EP-200158 | EP-200158 | 2015-10-24 |
| 00880304485105 | Active Articulation Hip System | EP-200160 | EP-200160 | 2015-10-24 |
| 00880304485112 | Active Articulation Hip System | EP-200162 | EP-200162 | 2015-10-24 |
| 00880304485129 | Active Articulation Hip System | EP-200164 | EP-200164 | 2015-11-04 |
| 00880304485136 | Active Articulation Hip System | EP-200166 | EP-200166 | 2015-10-24 |
| 00880304491328 | Active Articulation™ Dual Mobility Hip System | XL-200144 | XL-200144 | 2015-10-24 |
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|---|---|---|---|---|
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| 00811596033477 | CSR Shoulder System | CATALYST ORTHOSCIENCE INC. | KWT | 2026-09-22 |
| 00811596033484 | CSR Shoulder System | CATALYST ORTHOSCIENCE INC. | KWT | 2026-09-22 |
| 03701037320440 | FX V135 Shoulder Prosthesis | FX SOLUTIONS | KWT | 2026-09-22 |
| B1132N2GI200050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI200050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
| B1132N2GI200100 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
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| B1132N2GI220100 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI220100 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
| B1132N2GI226000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI226000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
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| B1132N2GI240050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI240050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
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| B1132N2GI246000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
| B1132N2GI246000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI248000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
| B1132N2GI248000 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |
| B1132N2GI270050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWT | 2026-09-18 |
| B1132N2GI270050 | Shoulder Innovations InSet GO | Shoulder Innovations, Inc. | KWS | 2026-09-18 |