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scalamobil®

FDA UDI

Class II (US FDA UDI)

by Alber GmbH

Identity

Trade Name
scalamobil® FDA UDI
Generic Name
Stairclimber FDA UDI
Model / Reference
S35 FDA UDI

Identifiers

Primary DI / UDI-DI
04046727148249 FDA UDI
510(k) Number
K920105 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

Yes

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

Yes

FDA UDI

Category: Stairclimber

scalamobil® by Alber 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

Manufacturer
Alber GmbH

Sources (1)

  • FDA UDI 03c940eb-10c7-4e73-b417-117418f7bffe 33 fields · synced Jun 8, 2026