Identity
- Trade Name
- VOLMED BRASIL FDA UDI
- Generic Name
- ENT surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- KIT FESS VOLMED FDA UDI
- Model / Reference
- 18-00-00-00 FDA UDI
- Description
- KIT FESS VOLMED FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07908783000534 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- ENT surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: ENT surgical procedure kit, non-medicated, single-useFluid transfer set, general-purpose
Volmed Brasil by Volmed Brasil Equipamentos Ltda — 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
- Volmed Brasil Equipamentos Ltda
Sources (1)
- FDA UDI ddc58a72-0104-432f-ae37-0ce07df478d6 33 fields · synced Jun 1, 2026