← Back to catalogue

ASTOR red line

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0014622-0002

by LAP GmbH Laser Applikationen

Identity

Trade Name
ASTOR red line EUDAMED
ASTOR FDA UDI
Generic Name
Laser patient positioning system FDA UDI
Device Name
Laser patient positioning system EUDAMED
Model / Reference
0014622-0002 EUDAMED
ASTOR red line FDA UDI

Identifiers

Catalog Number
0014622-0002 FDA UDI
Primary DI / UDI-DI
04260590370129 EUDAMEDFDA UDI
Basic UDI-DI
426059037PATPOSLASERCR EUDAMED
FDA Product Code
IWE FDA UDI
EMDN Code
Z119010 LASER SYSTEMS FOR PATIENT POSITIONING EUDAMED
GMDN Term
Laser patient positioning system FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
892.5780 FDA UDI
Market of Registration
Germany 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

No

FDA UDI

ASTOR red line by LAP GmbH Laser Applikationen — 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

EUDAMED SRN
DE-MF-000005792

Sources (2)

  • EUDAMED 7a9d2a44-c77c-47d5-89c3-09cf4251b472 61 fields · synced Jul 9, 2026
  • FDA UDI 07c521de-2622-4bee-ba39-02a1ae19a91d 33 fields · synced May 30, 2026