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Lumex

EUDAMEDFDA UDI

Class I (EU MDR)

Ref FR601P1325

by GF Health Products, Inc.

Identity

Trade Name
Lumex EUDAMEDFDA UDI
Generic Name
Reclining chair FDA UDI
Device Name
Clinical Care Recliners EUDAMED
RECL DLX CL CR PVT ARM ARMR FDA UDI
Model / Reference
FR601P1325 EUDAMEDFDA UDI
Description
RECL DLX CL CR PVT ARM ARMR FDA UDI

Identifiers

Primary DI / UDI-DI
M368FR601P13251 EUDAMEDFDA UDI
Basic UDI-DI
++M368CLINICALRECLINER2P EUDAMED
FDA Product Code
INM FDA UDI
EMDN Code
V080202 MANUAL MEDICAL CHAIRS EUDAMED
GMDN Term
Reclining chair FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.3100 FDA UDI
Market of Registration
Netherlands 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

Lumex by GF Health Products, Inc — 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

EUDAMED SRN
US-MF-000002167
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 8d7bff26-8208-44cb-a6bc-8d234498d17b 61 fields · synced Jul 28, 2026
  • FDA UDI 71332499-501b-4f50-8c76-262458fa9e64 34 fields · synced May 30, 2026