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TJO 3.2mm Classic Pin Puller

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2005.00.000

by Enztec Limited

Identity

Trade Name
TJO 3.2mm Classic Pin Puller EUDAMEDFDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
Pin Pullers EUDAMED
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
2005.00.000 EUDAMEDFDA UDI
Description
A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
2005.00.000 FDA UDI
Primary DI / UDI-DI
09421028110655 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN002529 EUDAMED
Direct Marketing DI
09421028110655 EUDAMED
FDA Product Code
HWB FDA UDI
EMDN Code
L0921 NON-IMPLANTABLE ORTHOPAEDIC DEVICES EXTRACTORS, REUSABLE EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
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

No

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

TJO 3.2mm Classic Pin Puller by Enztec Limited — 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

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Manufacturer

Manufacturer
Enztec Limited
EUDAMED SRN
NZ-MF-000002264
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 8bc3c001-fc4e-4b57-9697-e8db7a435e43 61 fields · synced Jul 18, 2026
  • FDA UDI 5ea0c09b-510d-44a9-abd0-2b5e1ceb4920 34 fields · synced May 30, 2026