Identity
- Trade Name
- ALLEN FDA UDI
- Generic Name
- Anaesthesia screen FDA UDI
- Device Name
- ANESTHESIA SCREEN, FLEXIBLE FDA UDI
- Model / Reference
- 101002 FDA UDI
- Description
- ANESTHESIA SCREEN, FLEXIBLE FDA UDI
Identifiers
- Catalog Number
- F-FAS FDA UDI
- Primary DI / UDI-DI
- 00615521014339 FDA UDI
- FDA Product Code
- FWZ FDA UDI
- GMDN Term
- Anaesthesia screen FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4950 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
Yes
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
Category: Anaesthesia screen
Allen by Hill-Rom, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthesia screen.
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- Anesthesia frame — Reison Medical AB · Class I
- Schaerer Medical USA — Schaerer Medical Usa, Inc. · Class I
- Schaerer Medical USA — Schaerer Medical Usa, Inc. · Class I
- DRAPE ROD, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
- Anesthesia screen — Skytron, LLC · Class I
- Anaesthesia screen extension — Maquet, Inc. · Class I
- Anesthesia frame — Reison Medical AB · Class I
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
- Hill-Rom, Inc.
Sources (1)
- FDA UDI 9710b720-e0b2-46ed-8bcd-0d528b877a0b 35 fields · synced May 30, 2026