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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
ENT wire-cutting scissors FDA UDI
Device Name
9" Pin Cutter Double Action, Angled, TC FDA UDI
Model / Reference
SD914277-1000 FDA UDI
Description
9" Pin Cutter Double Action, Angled, TC FDA UDI

Identifiers

Catalog Number
SD914277-1000 FDA UDI
Primary DI / UDI-DI
B382SD91427710000 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
ENT wire-cutting scissors 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: ENT wire-cutting scissors

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

Similar devices

Also classified as ENT wire-cutting scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5bce8196-da80-470f-85b6-e8eedb9cb963 35 fields · synced Jun 8, 2026