DISCOVERY ELBOW SYSTEM
- Primary DI
- 00880304005716
- Brand
- DISCOVERY ELBOW SYSTEM
- Company
- Biomet Orthopedics, LLC
- Model
- 114800
- Catalog number
- 114800
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304005716 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304005716 | 00880304005716 | 880304005716 | 0880304005716 |
GMDN Terms#
| Term | Definition |
|---|---|
| Metal-backed elbow ulna prosthesis | A sterile implantable device designed to replace the proximal ulna as part of an elbow joint replacement. The device is typically comprised of metal-backed polyethylene (PE) and its stem is usually coated with a material (e.g., porous materials, hydroxyapatite) intended to improve fixation and stability by promoting bone ingrowth. Fixation devices for implantation (e.g., screws) may be included and implantation may be performed with or without bone cement. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
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|---|---|---|---|---|
| 00889024706828 | Mini Baseplate Sizer Cannulated Handle | SSI008562 | SSI008562 | 2026-03-19 |
| 00889024706835 | Mini Baseplate Sizer 0 degree On-axis Handle | SSI008561 | SSI008561 | 2026-03-19 |
| 00887868551611 | StageOne Select | 431190 | 431190 | 2026-03-17 |
| 00887868551628 | StageOne Select | 431191 | 431191 | 2026-03-17 |
| 00887868551635 | StageOne Select | 431192 | 431192 | 2026-03-17 |
| 00887868551642 | StageOne Select | 431193 | 431193 | 2026-03-17 |
| 00887868551659 | StageOne Select | 431194 | 431194 | 2026-03-17 |
| 00887868551666 | StageOne Select | 431195 | 431195 | 2026-03-17 |
| 00887868551673 | StageOne Select | 431196 | 431196 | 2026-03-17 |
| 00887868551680 | StageOne Select | 431197 | 431197 | 2026-03-17 |
| 00887868551697 | StageOne Select | 431198 | 431198 | 2026-03-17 |
| 00887868551703 | STAGEONE SELECT | 431199 | 431199 | 2026-03-17 |
| 00889024706774 | Biomet® | 32-341692 | 32-341692 | 2026-03-12 |
| 00889024706781 | Biomet® | 32-148153 | 32-148153 | 2026-03-12 |
| 00889024706798 | Biomet® | 32-148151 | 32-148151 | 2026-03-12 |
| 00889024706804 | Biomet® | 32-341697 | 32-341697 | 2026-03-12 |
| 00889024706811 | Biomet® | 32-148149 | 32-148149 | 2026-03-12 |
| 00889024706484 | Vanguard® | 32-347021 | 32-347021 | 2026-02-27 |
| 00880304009615 | BMP CABLE CUTTER | 498010 | 498010 | 2020-05-23 |
| 00880304387676 | OPEN END CUTTER | 498023 | 498023 | 2020-05-23 |
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