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Krugg

EUDAMED

Class I (EU MDR)

Ref 959343Model TF-386

by Henry Schein Inc.

Identity

Trade Name
Krugg EUDAMED
Device Name
Examination Gloves EUDAMED
Model / Reference
TF-386 EUDAMED
959343 EUDAMED

Identifiers

Primary DI / UDI-DI
10304040134082 EUDAMED
Basic UDI-DI
03040438610DR EUDAMED
Unit of Use DI
00304040134085 EUDAMED
EMDN Code
T010201 LATEX EXAMINATION / TREATMENT GLOVES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

Reprocessed

Yes

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

Krugg by Henry Schein, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Henry Schein Inc.
EUDAMED SRN
US-MF-000021683
Authorised Representative
Henry Schein Services GmbH DE-AR-000008001

Sources (1)

  • EUDAMED 3731e7e0-49c0-4982-b2c4-b090fad141a8 61 fields · synced Jul 9, 2026