Identity
- Trade Name
- Medviron FDA UDI
- Generic Name
- Neonatal bed FDA UDI
- Device Name
- Bassinet Tub Service Part FDA UDI
- Model / Reference
- Bassinet Tub Service Part FDA UDI
- Description
- Bassinet Tub Service Part FDA UDI
Identifiers
- Catalog Number
- 523-0150-0000 FDA UDI
- Primary DI / UDI-DI
- 00851477007241 FDA UDI
- FDA Product Code
- NZG FDA UDI
- GMDN Term
- Neonatal bed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5145 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Neonatal bed
Medviron by Medviron Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Pedicraft — PEDICRAFT, INC. · Class II
- THE KERRI BEAR MATERNITY BASSINET — Imperial Surgical Ltd · Class II
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
- Medviron Llc
Sources (1)
- FDA UDI 49b32ca3-4689-4ec4-8590-6292c3337f34 35 fields · synced May 31, 2026