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Global Unite

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2100-01-040Model Orthopaedic Implant Aiming Arm

by DePuy Ireland UC

Identity

Trade Name
GLOBAL UNITE EUDAMEDFDA UDI
Generic Name
Orthopaedic implant aiming arm FDA UDI
Device Name
Orthopaedic Implant Aiming Arm EUDAMED
GLOBAL UNITE JIG CLAMP REPLACEMENT FDA UDI
Model / Reference
Orthopaedic Implant Aiming Arm EUDAMED
2100-01-040 EUDAMEDFDA UDI
Description
GLOBAL UNITE JIG CLAMP REPLACEMENT FDA UDI

Identifiers

Catalog Number
210001040 FDA UDI
Primary DI / UDI-DI
10603295085225 EUDAMEDFDA UDI
Basic UDI-DI
0603295a004198X EUDAMED
Direct Marketing DI
10603295085225 EUDAMED
FDA Product Code
HSD FDA UDI
KWS FDA UDI
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED
GMDN Term
Orthopaedic implant aiming arm FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
Market of Registration
Ireland 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

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

No

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: Orthopaedic implant impactor, reusable

Global Unite by DePuy Ireland UC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DePuy Ireland UC
EUDAMED SRN
IE-MF-000007377

Sources (2)

  • EUDAMED c2d109de-c946-42fa-8eb6-525eb887d976 61 fields · synced Jul 18, 2026
  • FDA UDI 3cfa6d27-8a21-44d3-881a-55fa3ee47370 35 fields · synced May 30, 2026