Identity
- Trade Name
- Aquasense FDA UDI
- Generic Name
- Bath back rest/seat FDA UDI
- Device Name
- AQS OPP 4" RAISED TO.SEAT, 1EA,3CV,Ret FDA UDI
- Model / Reference
- 770-610 FDA UDI
- Description
- AQS OPP 4" RAISED TO.SEAT, 1EA,3CV,Ret FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07540212104354 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
Yes
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: Bath back rest/seat
Aquasense by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bath back rest/seat.
- LUMEX — GF Health Products, Inc · Class I
- LUMEX — GF Health Products, Inc · Class I
- BIOS Living — Thermor Ltd · Class I
- LUMEX — GF Health Products, Inc · Class I
- DMI — DMS HOLDINGS, INC., · Class I
- R82 — R82 A/S · Class I
- R82 — R82 A/S · Class I
- INSPIRED — 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
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI c88f3754-6cab-4ab9-85f7-b483997be920 33 fields · synced Jun 8, 2026