← Back to catalogue

Thompson

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 6107Model Thompson Retractor System

by Thompson Surgical Instruments

Identity

Trade Name
Lap Inst Holder – All Universal Joints EUDAMED
Thompson FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Lap Inst Holder – All Universal Joints FDA UDI
Model / Reference
6107 EUDAMEDFDA UDI
Thompson Retractor System EUDAMED
Description
Lap Inst Holder – All Universal Joints FDA UDI

Identifiers

Primary DI / UDI-DI
00841536136418 EUDAMEDFDA UDI
Basic UDI-DI
008415361TRMR EUDAMED
Direct Marketing DI
00841536136418 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

Thompson by Thompson Surgical Instruments — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, 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 942b71ad-5b6c-4237-bf5f-ddf325d57f3f 34 fields · synced Jun 18, 2026
  • EUDAMED 03f325d6-4067-402d-8bcb-6c372fd4f7bd 61 fields · synced Jun 18, 2026