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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 1/2 inch Straight Plate and Wire Cutting Pliers - Replaced w/ SD14276.110 FDA UDI
Model / Reference
SDP11024 FDA UDI
Description
9 1/2 inch Straight Plate and Wire Cutting Pliers - Replaced w/ SD14276.110 FDA UDI

Identifiers

Catalog Number
SDP11024 FDA UDI
Primary DI / UDI-DI
B382SDP110240 FDA UDI
FDA Product Code
JEX FDA UDI
GMDN Term
ENT wire-cutting scissors 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: 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 6e2d9a8c-92ad-44a7-8dba-6eed20c7b059 35 fields · synced Jun 1, 2026