NA
- Primary DI
- 00889024458956
- Brand
- NA
- Company
- Zimmer, Inc.
- Model
- 32-5014-53
- Catalog number
- 32-5014-053-00
- Published
- 2016-09-05
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FTM | Mesh, surgical |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FTM | Mesh, Surgical | General, Plastic Surgery | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00889024458956 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889024458956 | 00889024458956 | 889024458956 | 0889024458956 |
GMDN Terms#
| Term | Definition |
|---|---|
| Multi-purpose surgical mesh, metallic | A sterile flat woven/knitted material made of a biocompatible metal (e.g., surgical stainless steel, tantalum) with appropriate mechanical characteristics for implantation. This non-dedicated device is used alone or in combination with synthetic materials (e.g., polymers) to support or protect tissues in reconstructive surgical procedures (e.g., to repair large chest wall defects or large abdominal incisional hernias) and/or orthopaedic procedures (e.g., cranioplasty, femoral reconstruction). Disposable devices associated with implantation (e.g., introducer needles, trocars) may be included. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)348-2759 | zimmer.consumerrelations@zimmer.com |
| +1(800)348-2759 | zimmer.consumerrelations@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 056038268
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00889024699854 | IDENTITY Humeral | 120001790 | 120001790 | 2026-10-21 |
| 00889024699861 | IDENTITY Humeral | 120001791 | 120001791 | 2026-10-21 |
| 00889024699878 | IDENTITY Humeral | 120001792 | 120001792 | 2026-10-21 |
| 00889024699885 | IDENTITY Humeral | 120001793 | 120001793 | 2026-10-21 |
| 00889024699892 | IDENTITY Humeral | 120001794 | 120001794 | 2026-10-21 |
| 00889024699908 | IDENTITY Humeral | 120001795 | 120001795 | 2026-10-21 |
| 00889024699915 | Comprehensive Humeral | 120001798 | 120001798 | 2026-10-21 |
| 00889024699922 | Identity Humeral | 120001799 | 120001799 | 2026-10-21 |
| 00889024699939 | N/A | 120002004 | 120002004 | 2026-10-20 |
| 00889024699946 | N/A | 120002005 | 120002005 | 2026-10-20 |
| 00889024699953 | Alliance Glenoid, Identity Humeral | 120006014 | 120006014 | 2026-10-20 |
| 00889024709164 | CANNULATED 1.5MM HEX DRIVER | SSI004137 | SSI004137 | 2026-10-19 |
| 00889024709171 | CANNULATED 2.0MM HEX DRIVER | SSI004138 | SSI004138 | 2026-10-19 |
| 00889024715196 | T6 Driver 127mm AO QC | SSI008712 | SSI008712 | 2026-10-19 |
| 00889024715202 | T8 Driver 127mm AO QC | SSI008713 | SSI008713 | 2026-10-19 |
| 00889024715295 | Persona Extended V/V Guide Assembly (MFS) | SSI008760 | SSI008760 | 2026-10-19 |
| 00889024715271 | Affixus® | 211306043 | 211306043 | 2026-10-06 |
| 00889024707160 | G7® Vivacit-E® | 30104005 | 30104005 | 2026-09-30 |
| 00889024707184 | G7® Vivacit-E® | 30103603 | 30103603 | 2026-09-30 |
| 00889024707207 | G7® Vivacit-E® | 30104407 | 30104407 | 2026-09-30 |
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| 00802526629914 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629921 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629938 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629945 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526630002 | EluPro™ | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526630019 | EluPro™ | Boston Scientific Corporation | FTM | 2026-05-27 |
| 09421907331881 | OviTex® Core | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331935 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331942 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331959 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331973 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222065 | OviTex® 2S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222096 | OviTex® Low Profile | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222102 | OviTex® Low Profile | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222157 | OviTex® Inguinal | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 00859389005331 | EluPro Antibiotic-Eluting BioEnvelope | Elutia Med LLC | FTM | 2024-09-06 |
| 00859389005348 | EluPro Antibiotic-Eluting BioEnvelope | Elutia Med LLC | FTM | 2024-09-06 |
| B454VSC10 | VersaWrap | Alafair Biosciences, Inc. | FTM | 2024-06-10 |
| 09421906661903 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 09421906661910 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 09421906661927 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 09421906661880 | Myriad Ultra™ Reinforced BioScaffold – Permanent (PP) | AROA BIOSURGERY LIMITED | FTM | 2022-11-28 |
| 09421906661897 | Myriad Ultra™ Reinforced BioScaffold – Permanent (PP) | AROA BIOSURGERY LIMITED | FTM | 2022-11-28 |
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