Identity
- Trade Name
- Sentient Manufacturing FDA UDI
- Generic Name
- Laser fibre stripper FDA UDI
- Device Name
- Sentient Manufacturing Laser Fiber Stripper FDA UDI
- Model / Reference
- 3041340 FDA UDI
- Description
- Sentient Manufacturing Laser Fiber Stripper FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860007603754 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Laser fibre stripper FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Sentient Manufacturing by Sentient Manufacturing , LLC — 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
- Sentient Manufacturing , LLC
Sources (1)
- FDA UDI f199bd5b-cef3-474d-9366-2f9215ada33c 34 fields · synced May 30, 2026