Identity
- Trade Name
- Susol® Partial Nail Avulsion Procedure Pack FDA UDI
- Generic Name
- Podiatry kit, single-use FDA UDI
- Model / Reference
- BSDP-03 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060418834890 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Podiatry kit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Podiatry kit, single-use
Susol® Partial Nail Avulsion Procedure Pack by Bailey Instruments Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Bailey Instruments Ltd
Sources (1)
- FDA UDI 1dbe0bc5-b3fa-46b0-98ea-ed516c54f314 32 fields · synced May 30, 2026