FREEDOM® ALL POLY CUP PROVISIONAL
- Primary DI
- 00880304516472
- Brand
- FREEDOM® ALL POLY CUP PROVISIONAL
- Company
- Biomet Orthopedics, LLC
- Model
- 31-117023
- Catalog number
- 31-117023
- Published
- 2020-05-15
- 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 |
|---|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304516472 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304516472 | 00880304516472 | 880304516472 | 0880304516472 |
GMDN Terms#
| Term | Definition |
|---|---|
| Acetabulum prosthesis trial, reusable | A copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically made of metal or polymer material and may be designed in the form of cages, shells, augments, or inserts. 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 |
|---|---|---|---|---|
| 00880304533424 | DVR® CrosslockWIDE PLATE RIGHT (HEAD WIDTH x OVERALL LENGTH) | 131813050 | 131813050 | 2015-10-24 |
| 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 |
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