Identity
- Trade Name
- Jiecang toilet lift FDA UDI
- Generic Name
- Patient lifting system toilet seat FDA UDI
- Model / Reference
- JC35LT1-1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06976169140519 FDA UDI
- FDA Product Code
- INO FDA UDI
- GMDN Term
- Patient lifting system toilet seat FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3110 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Patient lifting system toilet seat
Jiecang toilet lift by Zhejiang Dreamotion Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Zhejiang Dreamotion Technology Co., Ltd.
Sources (1)
- FDA UDI ea32deb0-cbbf-407c-933a-1554b0646a25 32 fields · synced May 30, 2026