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Bone Management

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 39MI102Model Surgical hand-held instruments

by Hager & Meisinger GmbH

Identity

Trade Name
Bone Management EUDAMED
n/a FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Manual instrument for dental/surgical application FDA UDI
Model / Reference
Surgical hand-held instruments EUDAMED
39MI102 EUDAMED
MI105 FDA UDI
Description
Manual instrument for dental/surgical application FDA UDI

Identifiers

Catalog Number
MI105 FDA UDI
Primary DI / UDI-DI
E0HM39MI1021 EUDAMEDFDA UDI
Basic UDI-DI
++E0HM209I04ABPW EUDAMED
Direct Marketing DI
E0HM39MI1021 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Bone Management by Hager & Meisinger GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000004966

Sources (2)

  • EUDAMED 730a14a7-25c9-49e6-9f5b-406070f2dfba 61 fields · synced Jun 9, 2026
  • FDA UDI c94634a3-3bb3-4277-ae29-542e04c54345 35 fields · synced May 30, 2026