← Back to catalogue

45656a

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 45656AModel Thompson Retractor System

by Thompson Surgical Instruments, Inc.

Identity

Trade Name
Thompson FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Malleable 25x110mm FDA UDI
Model / Reference
Thompson Retractor System EUDAMED
45656A EUDAMEDFDA UDI
Description
Malleable 25x110mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841536113280 EUDAMEDFDA UDI
Basic UDI-DI
008415361TRMR EUDAMED
Direct Marketing DI
00841536113280 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 retraction system, reusable

45656a by Thompson Surgical Instruments, Inc. — Class IIa — 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-000013232
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 809c64c7-b329-45b8-a89e-3106c62b4ba8 61 fields · synced Jul 13, 2026
  • FDA UDI ad97af93-116e-439f-8a3d-6d3139ef5d69 34 fields · synced May 30, 2026