Comprehensive® VRS Glenoid
- Primary DI
- 00880304818965
- Brand
- Comprehensive® VRS Glenoid
- Company
- Biomet Orthopedics, LLC
- Model
- 110031178
- Catalog number
- 110031178
- Published
- 2020-05-23
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| PHX | shoulder prosthesis, reverse configuration |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| PHX | Shoulder Prosthesis, Reverse Configuration | Orthopedic | 2 |
Premarket Submissions#
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304818965 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304818965 | 00880304818965 | 880304818965 | 0880304818965 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic reamer guide | An orthopaedic surgical device that functions as a guide for an orthopaedic reamer. The guide, commonly called a spigot, is inserted into a predetermined site where bone is to be resected for the acceptance of a prosthetic implant, typically at or within a joint (e.g., the condyle head of the knee, the olecranon of the ulna) or for the reaming of the intramedullary canal for acceptance of an intramedullary nail. The device allows the controlled cutting action of the reamer which is steered down its length. It is typically made of a high-grade stainless steel alloy; it comes in varying sizes. This is a reusable device. |
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
- Expiration date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888480584162 | PRO OSTEON 200 | 2B040 | 2B040 | 2015-10-24 |
| 00888480584179 | PRO OSTEON 200 | 2B045 | 2B045 | 2015-10-24 |
| 00888480584186 | PRO OSTEON 200 | 2B075 | 2B075 | 2015-10-24 |
| 00888480584247 | PRO OSTEON 200 | 2G02 | 2G02 | 2015-10-24 |
| 00888480584254 | PRO OSTEON 200 | 2G05 | 2G05 | 2015-10-24 |
| 00888480584339 | PRO OSTEON 200R | 2RG005 | 2RG005 | 2015-10-24 |
| 00888480584346 | PRO OSTEON 200R | 2RG02 | 2RG02 | 2015-10-24 |
| 00888480584353 | PRO OSTEON 200R | 2RG05 | 2RG05 | 2015-10-24 |
| 00888480584360 | PRO OSTEON 200R | 2RG15 | 2RG15 | 2015-10-24 |
| 00888480584476 | PRO OSTEON 500 | 5B040 | 5B040 | 2015-10-24 |
| 00888480584483 | PRO OSTEON 500 | 5B075 | 5B075 | 2015-10-24 |
| 00888480584490 | PRO OSTEON 500 | 5B100 | 5B100 | 2015-10-24 |
| 00888480584575 | PRO OSTEON 500 | 5G05 | 5G05 | 2015-10-24 |
| 00888480584582 | PRO OSTEON 500 | 5G10 | 5G10 | 2015-10-24 |
| 00888480584599 | PRO OSTEON 500 | 5G15 | 5G15 | 2015-10-24 |
| 00888480584629 | PRO OSTEON 500 | 5G30 | 5G30 | 2015-10-24 |
| 00888480584681 | PRO OSTEON 500R | 5RB010 | 5RB010 | 2015-10-24 |
| 00888480584698 | PRO OSTEON 500R | 5RB014 | 5RB014 | 2015-10-24 |
| 00888480584704 | PRO OSTEON 500R | 5RB024 | 5RB024 | 2015-10-24 |
| 00888480584711 | PRO OSTEON 500R | 5RB040 | 5RB040 | 2015-10-24 |
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