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Trephine Φ2.7

EUDAMED

Class I (EU MDR)

Ref F16BB-PA00768

by Wuhan Mindray Scientific Co., Ltd.

Identity

Trade Name
Trephine Φ2.7 EUDAMED
Device Name
Non-sterile Orthopedic Manual Surgical Instruments EUDAMED
Model / Reference
F16BB-PA00768 EUDAMED

Identifiers

Primary DI / UDI-DI
06934635740991 EUDAMED
Basic UDI-DI
B-06934635740991 EUDAMED
EMDN Code
L090902 ORTHOPAEDIC SURGERY TREPHINES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Bone trephine, reusable

Trephine Φ2.7 by Wuhan Mindray Scientific Co., Ltd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone trephine, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000032692
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8bbc3a64-ba92-416d-b1b7-580cc287baa2 61 fields · synced Jun 19, 2026