← Back to catalogue

Fixed Hudson T-Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref II-1-0328

by Integrity Implants Inc.

Identity

Trade Name
Fixed Hudson T-Handle EUDAMED
NA FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
FlareHawk Handles EUDAMED
Fixed Hudson T-Handle FDA UDI
Model / Reference
II-1-0328 EUDAMEDFDA UDI
Description
Fixed Hudson T-Handle FDA UDI

Identifiers

Catalog Number
II-1-0328 FDA UDI
Primary DI / UDI-DI
00818613020083 EUDAMEDFDA UDI
Basic UDI-DI
0081000472HANDLESMF EUDAMED
Direct Marketing DI
00818613020083 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Category: Surgical retraction system, reusable

Fixed Hudson T-Handle by Integrity Implants Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

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
US-MF-000009805
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 1b6e2755-7f5f-43d7-82e4-1f3e6e90439f 61 fields · synced Jun 19, 2026
  • FDA UDI dae85722-af98-4179-bcf3-565eca3887f5 35 fields · synced May 30, 2026