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Liftkar®

FDA UDI

Class II (US FDA UDI)

by Sano Transportgeraete GmbH

Identity

Trade Name
LIFTKAR® FDA UDI
Generic Name
Stairclimber FDA UDI
Model / Reference
PT Universal 160 FDA UDI

Identifiers

Primary DI / UDI-DI
09120047770283 FDA UDI
510(k) Number
K110495 FDA UDI
FDA Product Code
ING FDA UDI
GMDN Term
Stairclimber FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3930 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stairclimber

Liftkar® by Sano Transportgeraete GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stairclimber.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e254dff-bd11-480f-b3b8-41cf29386358 33 fields · synced May 30, 2026