Identity
- Trade Name
- Bassinet FDA UDI
- Generic Name
- Neonatal bed FDA UDI
- Device Name
- Bassinet FDA UDI
- Model / Reference
- P247E FDA UDI
- Description
- Bassinet FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00887761996922 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Neonatal bed
Bassinet by Hill-Rom, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Neonatal bed.
- NB-SSxB — Novum Medical Products · Class II
- Pedicraft — PEDICRAFT, INC. · Class II
- Amico Patient Care Corporation — Amico Patient Care Corporation · Class II
- Amico Patient Care Corporation — Amico Patient Care Corporation · Class II
- CUB — Stryker Corp. · Class II
- 9201-C — Novum Medical Products · Class II
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hill-Rom, Inc.
Sources (1)
- FDA UDI c2f3b4c4-2e5b-4247-8bd7-bc6ae68ab065 34 fields · synced May 30, 2026