← Back to catalogue

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
4 1/2 inch Iris Scissors Curved, TC, Super Cut FDA UDI
Model / Reference
SD903985110SC FDA UDI
Description
4 1/2 inch Iris Scissors Curved, TC, Super Cut FDA UDI

Identifiers

Catalog Number
SD903985110SC FDA UDI
Primary DI / UDI-DI
B382SD903985110SC0 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

Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Surgical Direct, Inc.

Sources (1)

  • FDA UDI 40ae4114-103d-43e3-9fa4-97e78a0d1300 35 fields · synced Jun 8, 2026