← Back to catalogue

Target

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 232004Model Hamstring Trephines

by Medos International Sàrl

Identity

Trade Name
TARGET TENDON HARVESTER INSTRUMENT EUDAMED
TARGET FDA UDI
Generic Name
Bone trephine, reusable FDA UDI
Device Name
Tendon Harvester, TARGET EUDAMED
TARGET TENDON HARVESTER INSTRUMENT FDA UDI
Model / Reference
232004 EUDAMEDFDA UDI
Hamstring Trephines EUDAMED
Description
TARGET TENDON HARVESTER INSTRUMENT FDA UDI

Identifiers

Catalog Number
232004 FDA UDI
Primary DI / UDI-DI
10886705010905 EUDAMEDFDA UDI
Basic UDI-DI
0886705a00138KM EUDAMED
Direct Marketing DI
10886705010905 EUDAMED
FDA Product Code
NBH FDA UDI
EMDN Code
L091399 ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER EUDAMED
GMDN Term
Bone trephine, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.1100 FDA UDI
Market of Registration
Belgium 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

Yes

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

Category: Bone trephine, reusable

Target by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone trephine, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI a1888086-6828-4bc4-b0c2-757b54860e0f 35 fields · synced Jul 15, 2026
  • EUDAMED 88b254be-3b08-4a16-933a-e7ac58fc03c7 61 fields · synced Jul 15, 2026