Identity
- Trade Name
- Instrument kit FDA UDI
- Generic Name
- Joint prosthesis implantation kit, reusable FDA UDI
- Device Name
- Even Cross Connect Acetabular Reamers Kit FDA UDI
- Model / Reference
- Instrument kit FDA UDI
- Description
- Even Cross Connect Acetabular Reamers Kit FDA UDI
Identifiers
- Catalog Number
- IF07000 FDA UDI
- Primary DI / UDI-DI
- 08054752863231 FDA UDI
- GMDN Term
- Joint prosthesis implantation kit, reusable FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Joint prosthesis implantation kit, reusable
Instrument kit by Adler Ortho Spa — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Joint prosthesis implantation kit, reusable.
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- Evolution — MicroPort Orthopedics Inc. · Class II
- GUARDIAN® — MicroPort Orthopedics Inc. · Class I
- ADVANCE® — MicroPort Orthopedics Inc. · Class I
- PROPHECY — MicroPort Orthopedics Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
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Manufacturer
- Manufacturer
- Adler Ortho Spa
Sources (1)
- FDA UDI c1b9da00-1a9b-4a3a-9a9b-4bc6510ef4c8 34 fields · synced Jun 8, 2026