← Back to catalogue

Thompson

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 46211Model Thompson Retractor System

by Thompson Surgical Instruments

Identity

Trade Name
Volkman Blunt 6 Png 25x13mm EUDAMED
Thompson FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Volkman Blunt 6 Png 25x13mm FDA UDI
Model / Reference
46211 EUDAMEDFDA UDI
Thompson Retractor System EUDAMED
Description
Volkman Blunt 6 Png 25x13mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841536116595 EUDAMEDFDA UDI
Basic UDI-DI
008415361TRMR EUDAMED
Direct Marketing DI
00841536116595 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical retractor/retraction system blade, 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 retractor/retraction system blade, 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 retractor/retraction system blade, 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 ad8316d3-25f8-432b-b049-6654f0b669aa 34 fields · synced Jul 14, 2026
  • EUDAMED 57a8d86b-2553-413d-83ad-d6164b8acf37 61 fields · synced Jul 14, 2026