Identity
- Trade Name
- Daniels FDA UDI
- Generic Name
- Surgical instrument interim-placement holder, single-use FDA UDI
- Device Name
- Bladesafe Multi Sterile FDA UDI
- Model / Reference
- 4503601004 FDA UDI
- Description
- Bladesafe Multi Sterile FDA UDI
Identifiers
- Primary DI / UDI-DI
- 09333990005009 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Surgical instrument interim-placement holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Daniels by Daniels Corporation International Pty Ltd — 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
- Daniels Corporation International Pty Ltd
Sources (1)
- FDA UDI e66007da-2d6a-43ab-8e6d-5869541be325 34 fields · synced Jun 6, 2026