Identity
- Trade Name
- Barricaid ACD Impactor FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- Reusable impactor designed to further advance the Barricaid Anular Closure Device (ACD) anchor into the vertebral body, if during the implantation the satisfactory depth has not been achieved and the Barricaid delivery tool has already been removed. FDA UDI
- Model / Reference
- 400906 FDA UDI
- Description
- Reusable impactor designed to further advance the Barricaid Anular Closure Device (ACD) anchor into the vertebral body, if during the implantation the satisfactory depth has not been achieved and the Barricaid delivery tool has already been removed. FDA UDI
Identifiers
- Catalog Number
- IMP-1-A FDA UDI
- Primary DI / UDI-DI
- M906IMP1A0 FDA UDI
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Classification
- Commercial Distribution
- Not 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
Barricaid ACD Impactor by Intrinsic Therapeutics — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 fb368111-8d1c-4f6a-9700-cdb78c3c8b41 35 fields · synced Jun 6, 2026