Identity
- Trade Name
- TACIT QUICKANCHOR ETHIBOND TAPERCUT FDA UDI
- Generic Name
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
- Device Name
- TACIT QUICKANCHOR (Cranio Drill) 2.0mm Size 2/0 white ETHIBOND braided polyester suture, 18 Inches (45 cm), double-armed with V-5 TAPERCUT needles, with disposable inserter and 1.7mm x 4.0mm Cranio Drill. FDA UDI
- Model / Reference
- 212236 FDA UDI
- Description
- TACIT QUICKANCHOR (Cranio Drill) 2.0mm Size 2/0 white ETHIBOND braided polyester suture, 18 Inches (45 cm), double-armed with V-5 TAPERCUT needles, with disposable inserter and 1.7mm x 4.0mm Cranio Drill. FDA UDI
Identifiers
- Catalog Number
- 212236 FDA UDI
- Primary DI / UDI-DI
- 10886705002023 FDA UDI
- FDA Product Code
- MBI FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Tacit Quickanchor Ethibond Tapercut by DePuy Mitek, Inc. — Class II — 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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- DePuy Mitek, Inc.
Sources (1)
- FDA UDI 0b630606-6986-4655-8c1c-cd7eb91fcf85 37 fields · synced May 31, 2026