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Molift RgoSling Active

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1720920Model Sling

by Etac A/S

Identity

Trade Name
Molift RgoSling Active EUDAMED
Molift FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Model / Reference
Sling EUDAMED
1720920 EUDAMED
Molift RgoSling Active S FDA UDI

Identifiers

Catalog Number
1720920 FDA UDI
Primary DI / UDI-DI
05707995000552 EUDAMEDFDA UDI
Basic UDI-DI
570799525TP EUDAMED
FDA Product Code
IKX FDA UDI
EMDN Code
Y1299 PERSONAL MOBILITY DEVICES - OTHER EUDAMED
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.5050 FDA UDI
Market of Registration
Denmark EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Molift RgoSling Active by Etac A/S — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Etac A/S
EUDAMED SRN
DK-MF-000017724

Sources (2)

  • EUDAMED 5e751909-8071-4bfd-ade4-461c6b9a6ec8 61 fields · synced Jul 13, 2026
  • FDA UDI d74c4e2e-125e-45b6-bd14-433a4c0dabe9 33 fields · synced May 30, 2026