Identity
- Trade Name
- Anchor Down Cutting Straight Curette, 3x5mm FDA UDI
- Generic Name
- Neurosurgical curette, single-use FDA UDI
- Model / Reference
- PSZ-400-306 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00685447002093 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Neurosurgical curette, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Anchor Down Cutting Straight Curette, 3x5mm by Baylis Médicale Cie 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
- Baylis Médicale Cie Inc
Sources (1)
- FDA UDI 94a88d6a-8d41-497f-a07a-34c30b310c27 34 fields · synced Jun 1, 2026