← Back to catalogue

scalacombi S39

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1566816Model scalacombi S39

by Alber GmbH

Identity

Trade Name
scalacombi S39 EUDAMED
scalamobil® FDA UDI
Generic Name
Stairclimber FDA UDI
Device Name
scalacombi S39 EUDAMED
Model / Reference
scalacombi S39 EUDAMED
1566816 EUDAMED
S35 FDA UDI

Identifiers

Primary DI / UDI-DI
04046727172138 EUDAMEDFDA UDI
Basic UDI-DI
4046727scalacombiS396K EUDAMED
510(k) Number
K920105 FDA UDI
FDA Product Code
ING FDA UDI
EMDN Code
Y183012 MOBILE STAIRLIFTS EUDAMED
GMDN Term
Stairclimber FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.3930 FDA UDI
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

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

scalacombi S39 by Alber GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Alber GmbH
EUDAMED SRN
DE-MF-000005502

Sources (2)

  • EUDAMED 9892b5ff-ec20-4750-a809-9be329dfffa2 61 fields · synced Jul 18, 2026
  • FDA UDI 3de69e59-a3d7-40e4-a636-da02e2519884 33 fields · synced May 29, 2026