Identity
- Trade Name
- CUSTOM FDA UDI
- Generic Name
- Surgical depth gauge, reusable FDA UDI
- Device Name
- CANNULATED TAP FOR 1/4 POWERED DRILL DEVICE Ø 7.5mm FDA UDI
- Model / Reference
- A99131075 FDA UDI
- Description
- CANNULATED TAP FOR 1/4 POWERED DRILL DEVICE Ø 7.5mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03613720223283 FDA UDI
- FDA Product Code
- HWX FDA UDI
- GMDN Term
- Surgical depth gauge, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- 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
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
Moist Heat or Steam Sterilization FDA UDI
Custom by Medicrea International SA — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medicrea International SA
Sources (1)
- FDA UDI 62918cd8-6bd7-4434-bfb5-a1547387ebc1 34 fields · synced Jun 8, 2026