← Back to catalogue

Thompson

FDA UDI

Class II (US FDA UDI)

by Thompson Surgical Instruments

Identity

Trade Name
Thompson FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Skull Clamp Mount w/Cam Joint FDA UDI
Model / Reference
44232 FDA UDI
Description
Skull Clamp Mount w/Cam Joint FDA UDI

Identifiers

Primary DI / UDI-DI
00841536134230 FDA UDI
510(k) Number
K210615 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

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 II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Cleared under the same submission

K210615 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Thompson Surgical Instruments

Sources (1)

  • FDA UDI 1bdbad9a-f179-42d8-a529-d20758de57b1 35 fields · synced May 30, 2026