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Hudson - Large Ao Adaptor

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 900020112

by Enztec Limited

Identity

Trade Name
HUDSON - LARGE AO ADAPTOR EUDAMED
Hudson Large AO Adaptor FDA UDI
Generic Name
Surgical power tool adaptor FDA UDI
Device Name
Surgical Power Tool Attachments EUDAMED
A surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI
Model / Reference
900020112 EUDAMEDFDA UDI
Description
A surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI

Identifiers

Catalog Number
900020112 FDA UDI
Primary DI / UDI-DI
09421028118583 EUDAMEDFDA UDI
Basic UDI-DI
942102811GMN00282F EUDAMED
FDA Product Code
HWE FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical power tool adaptor FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4820 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

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

Hudson - Large Ao Adaptor by Enztec Limited — Class IIa — 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 ca05e7a3-8c7e-49be-8633-d4d7c2c76366 61 fields · synced Jul 12, 2026
  • FDA UDI 48b69f5b-0b6e-4d8c-9a0a-3696acd41869 34 fields · synced May 30, 2026