Identity
- Trade Name
- Barricaid® ACD Retraction Wedge FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- Wedge to aid in retraction of the delivery tool following implantation of the Barricaid® Annular Closure Device (ACD). Reusable wedge designed to help pull back the strike cap following full Barricaid deployment. FDA UDI
- Model / Reference
- 400846 FDA UDI
- Description
- Wedge to aid in retraction of the delivery tool following implantation of the Barricaid® Annular Closure Device (ACD). Reusable wedge designed to help pull back the strike cap following full Barricaid deployment. FDA UDI
Identifiers
- Catalog Number
- BAR-WEDGE FDA UDI
- Primary DI / UDI-DI
- M906BARWEDGE0 FDA UDI
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, 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
No
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: Orthopaedic prosthesis implantation positioning instrument, reusable
Barricaid® ACD Retraction Wedge by Intrinsic Therapeutics — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Intrinsic Therapeutics
Sources (1)
- FDA UDI 0593d2f0-e5b5-4959-bae7-260d64a79ebe 35 fields · synced May 30, 2026