Identity
- Trade Name
- Sittan FDA UDI
- Generic Name
- Overbed table FDA UDI
- Device Name
- Mechanical table to support a patient with the right position FDA UDI
- Model / Reference
- KF-890UW FDA UDI
- Description
- Mechanical table to support a patient with the right position FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04527799705993 FDA UDI
- FDA Product Code
- IKX FDA UDIINW FDA UDI
- GMDN Term
- Overbed table FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 FDA UDI890.3750 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Overbed table
Sittan by Paramount Bed Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Overbed table.
- AMFAB — Drive Devilbiss Healthcare · Class I
- DALTON OVERBED TABLE — Dalton Medical Corp. · Class I
- AMFAB — Drive Devilbiss Healthcare · Class I
- AMFAB — Drive Devilbiss Healthcare · Class I
- AMFAB — Drive Devilbiss Healthcare · Class I
- AMFAB — Drive Devilbiss Healthcare · Class I
- AMFAB — Drive Devilbiss Healthcare · Class I
- AMFAB — Drive Devilbiss Healthcare · 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
- Paramount Bed Co., Ltd.
Sources (1)
- FDA UDI ba1caeae-8e83-486f-9797-7152daaa5497 33 fields · synced May 30, 2026