Identity
- Trade Name
- Anesthesia frame FDA UDI
- Generic Name
- Anaesthesia screen FDA UDI
- Model / Reference
- 10-311-US FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07350111830946 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
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
Category: Anaesthesia screen
Anesthesia frame by Reison Medical AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Anaesthesia screen.
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- DRAPE ROD, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
- Anesthesia screen — Skytron, LLC · Class I
- Anaesthesia screen extension — Maquet, Inc. · Class I
- Mindray — Nanjing Mindray Bio-Medical Electronics Co., Ltd · 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
- Reison Medical AB
Sources (1)
- FDA UDI b12895f0-949c-4155-b69e-a314867fdfa5 32 fields · synced Jun 6, 2026