Identity
- Trade Name
- DMI FDA UDI
- Generic Name
- Bath back rest/seat FDA UDI
- Device Name
- BARIATRIC BATH SEAT W/BACK FDA UDI
- Model / Reference
- 522-1816-1999 FDA UDI
- Description
- BARIATRIC BATH SEAT W/BACK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00041298524113 FDA UDI
- FDA Product Code
- ILS FDA UDI
- GMDN Term
- Bath back rest/seat FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bath back rest/seat
Dmi by Dms Holdings, Inc., — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bath back rest/seat.
- INSPIRED — Drive Devilbiss Healthcare · Class I
- INSPIRED — Drive Devilbiss Healthcare · Class I
- Aquasense — Drive Devilbiss Healthcare · Class I
- INSPIRED — Drive Devilbiss Healthcare · Class I
- INSPIRED — Drive Devilbiss Healthcare · Class I
- LUMEX — GF Health Products, Inc · Class I
- Aquasense — Drive Devilbiss Healthcare · Class I
- DRIVEMEDICAL — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dms Holdings, Inc.,
Sources (1)
- FDA UDI fa058ca0-0b6c-4c1e-9268-13acb4462083 33 fields · synced Jun 8, 2026