← Back to catalogue

Kilner Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
KILNER SCISSORS FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
KILNER SCISSORS STRAIGHT BLADE POWER CUT BLACK FDA UDI
Model / Reference
2400-443 FDA UDI
Description
KILNER SCISSORS STRAIGHT BLADE POWER CUT BLACK FDA UDI

Identifiers

Catalog Number
2400-443 FDA UDI
Primary DI / UDI-DI
00192896098459 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, 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

Yes

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

Dimensions & Sizes

Size
Length — 4.875 Inch FDA UDI

Category: General-purpose surgical scissors, reusable

Kilner Scissors by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical scissors, reusable.

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

Sources (1)

  • FDA UDI 2ede9022-24e5-4792-a31c-0ed9d23534d0 36 fields · synced May 30, 2026