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Applicator

EUDAMED

Class I (EU MDR)

Ref Rule 1

by Ningbo Tianbo First Aid Product Co., Ltd.

Identity

Device Name
Applicator EUDAMED
Model / Reference
Rule 1 EUDAMED

Identifiers

Primary DI / UDI-DI
06974712705208 EUDAMED
Basic UDI-DI
697471270TBMQ01NV EUDAMED
Direct Marketing DI
06974712705208 EUDAMED
EMDN Code
Q019003 DENTAL FLOSS AND OTHER DEVICES FOR ORAL HYGIENE (FOR PROFESSIONAL USE) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Applicator by Ningbo Tianbo First Aid Product Co., Ltd. — 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

EUDAMED SRN
CN-MF-000016721
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 13062e42-73d0-457b-914b-58ebb7620696 61 fields · synced Jul 17, 2026