Identity
- Trade Name
- NOVO Health Services, LLC FDA UDI
- Generic Name
- Emesis bowl, reusable FDA UDI
- Device Name
- EYE BOWL, 900CC FDA UDI
- Model / Reference
- 123122 FDA UDI
- Description
- EYE BOWL, 900CC FDA UDI
Identifiers
- Catalog Number
- 123122 FDA UDI
- Primary DI / UDI-DI
- 00812564032812 FDA UDI
- FDA Product Code
- FNY FDA UDI
- GMDN Term
- Emesis bowl, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6730 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Weight — 0.3 Pound FDA UDIWidth — 8 Inch FDA UDIHeight — 3 Inch FDA UDI
NOVO Health Services, LLC by Novo Health Services, Llc — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Novo Health Services, Llc
Sources (1)
- FDA UDI 6950f384-d7e9-4ba1-9c4f-28d47f7086a8 37 fields · synced May 30, 2026