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Thompson

FDA UDI

Class II (US FDA UDI)

by Thompson Surgical Instruments

Identity

Trade Name
Thompson FDA UDI
Generic Name
Neurosurgical retraction system, brain FDA UDI
Device Name
Brain Retractor 9x102mm FDA UDI
Model / Reference
47111 FDA UDI
Description
Brain Retractor 9x102mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841536118575 FDA UDI
510(k) Number
K210615 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Neurosurgical retraction system, brain 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: Neurosurgical retraction system, brain

Thompson by Thompson Surgical Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical retraction system, brain.

Cleared under the same submission

K210615 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thompson Surgical Instruments

Sources (1)

  • FDA UDI a502b74f-8495-4f33-a0ca-256f5728f2b4 35 fields · synced May 30, 2026