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Molift

FDA UDI

Class I (US FDA UDI)

by Etac A/S

Identity

Trade Name
Molift FDA UDI
Generic Name
Standing transfer platform, manual FDA UDI
Model / Reference
Molift Soft Handles 2 pcs FDA UDI

Identifiers

Catalog Number
82511 FDA UDI
Primary DI / UDI-DI
05707995002068 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Standing transfer platform, manual 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Standing transfer platform, manual

Molift by Etac A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Standing transfer platform, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Etac A/S

Sources (1)

  • FDA UDI c0134538-baeb-4fab-94bb-1312e95f1efb 33 fields · synced Jun 1, 2026