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310/B-3 Height Adjustable Mobile Shield

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 310/B-3/91

by Kenex (Electro-Medical) Limited

Identity

Trade Name
310/B-3 Height Adjustable Mobile Shield EUDAMED
KENEX FDA UDI
Generic Name
Radiation shielding panel, portable/mobile FDA UDI
Device Name
Mobile and portable radiation shield panels EUDAMED
Shield 310/B-3 With 769x8x25mm Rail FDA UDI
Model / Reference
310/B-3/91 EUDAMEDFDA UDI
Description
Shield 310/B-3 With 769x8x25mm Rail FDA UDI

Identifiers

Catalog Number
310/B-3/91 FDA UDI
Primary DI / UDI-DI
05055449402675 EUDAMEDFDA UDI
Basic UDI-DI
50554494SHMXK EUDAMED
FDA Product Code
IWX FDA UDI
EMDN Code
T0399 PROTECTION DEVICES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT PPE) - OTHER EUDAMED
GMDN Term
Radiation shielding panel, portable/mobile FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
892.6500 FDA UDI
Market of Registration
Northern Ireland 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

Yes

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

310/B-3 Height Adjustable Mobile Shield by Kenex (electro-Medical) Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000009022
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 07e13dc1-7ade-4bcd-b98a-75f80b0fca53 61 fields · synced Jun 19, 2026
  • FDA UDI 09fdd293-dc9b-44c5-a1f5-b032eb158ff3 34 fields · synced May 30, 2026