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Surgical Direct

FDA UDI

Class I (US FDA UDI)

by Surgical Direct, Inc.

Identity

Trade Name
Surgical Direct FDA UDI
Generic Name
General-purpose surgical scissors, single-use FDA UDI
Device Name
9 inch Jorgenson Scissors, Curved FDA UDI
Model / Reference
SD903366100 FDA UDI
Description
9 inch Jorgenson Scissors, Curved FDA UDI

Identifiers

Catalog Number
SD903366100 FDA UDI
Primary DI / UDI-DI
B382SD9033661000 FDA UDI
FDA Product Code
EGN FDA UDI
GMDN Term
General-purpose surgical scissors, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical scissors, single-use

A comprehensive 2-3 paragraph SEO description written in clear, natural language. The device is designed to be a single-use hand-held manual surgical instrument for cutting and dissecting tissues during open surgery. It features pivoted shearing blades with handles, allowing the user to make precise cuts without having to manually manipulate the blades.

Similar devices

Also classified as General-purpose surgical scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgical Direct, Inc.

Sources (1)

  • FDA UDI 3848f0af-6f48-445a-af35-8b5ddf10ab60 35 fields · synced Jun 22, 2026