Thompson

FDA UDI

Class I (US FDA UDI)

by Thompson Surgical Instruments

Identity

Trade Name: Thompson FDA UDI
Generic Name: Surgical retraction system, reusable FDA UDI
Device Name: Fine Vessel 1.5mm - 120mm FDA UDI
Model / Reference: SL44392 FDA UDI
Description: Fine Vessel 1.5mm - 120mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00841536127997 FDA UDI
510(k) Number: K151347 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Surgical retraction system, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

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

Similar devices

Also classified as Surgical retraction system, reusable.

45930R — Thompson Surgical Instruments, Inc. · Class IIa
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Nordent Manufacturing, Inc. — NORDENT MANUFACTURING INC · Class I
GRACEY 14 TALON TOUGH QUIK TIP — American Eagle Instruments · Class I
Falcon — Falcon Surgical Co. (Pvt.) Ltd · Class I
Straight stem trial , PSA , Ø10 × 100mm — NORMMED MEDİKAL SAN. VE TİC. A.Ş. · Class I

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Thompson Surgical Instruments

Sources (1)

FDA UDI c199208b-06ae-4518-898e-bb86d49d4030 34 fields · synced May 31, 2026