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Thompson

FDA UDI

Class I (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
Rot Soft Malleable 76 x 254mm FDA UDI
Model / Reference
45024AS FDA UDI
Description
Rot Soft Malleable 76 x 254mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841536110630 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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 surgical retractor/retraction system blade, a reusable and variable length metal device designed to assist in separating the margins of a wound/incision during a surgical procedure. It is part of a comprehensive surgical instrument kit and intended for implantation in general plastic surgery.

Similar devices

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

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 d31ec794-464d-4af0-ad2d-2bae7e19132d 34 fields · synced Jul 24, 2026