Identity
- Trade Name
- DALTON PATIENT LIFT FDA UDI
- Generic Name
- Mobile patient lifting system, line-powered FDA UDI
- Device Name
- PATIENT LIFT, ELECTRIC, WT. LIMIT 400 lbs. FDA UDI
- Model / Reference
- PL4200E-S FDA UDI
- Description
- PATIENT LIFT, ELECTRIC, WT. LIMIT 400 lbs. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815027011713 FDA UDI
- FDA Product Code
- FNG FDA UDI
- GMDN Term
- Mobile patient lifting system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5500 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Mobile patient lifting system, line-powered
Dalton Patient Lift by Dalton Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mobile patient lifting system, line-powered.
- DALTON PATIENT LIFT — Dalton Medical Corp. · Class II
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 |
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Manufacturer
- Manufacturer
- Dalton Medical Corp.
Sources (1)
- FDA UDI def8f6bd-3254-44e4-beba-6504861fae9e 34 fields · synced May 31, 2026