Carnegie Surgical LLC

FDA UDI

Class I (US FDA UDI)

by Carnegie Surgical LLC

Identity

Trade Name: Carnegie Surgical LLC FDA UDI
Generic Name: General-purpose surgical scissors, reusable FDA UDI
Device Name: Trepsat Facial Flap Dissector Scissors, Supercut, Straight, Size Medium, Blade (15mm x 25mm), Length 18 cm FDA UDI
Model / Reference: 572-1518 FDA UDI
Description: Trepsat Facial Flap Dissector Scissors, Supercut, Straight, Size Medium, Blade (15mm x 25mm), Length 18 cm FDA UDI

Identifiers

Catalog Number: 572-1518 FDA UDI
Primary DI / UDI-DI: G14157215180 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical scissors, reusable

Carnegie Surgical LLC by Carnegie Surgical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Carnegie Surgical LLC

Sources (1)

FDA UDI f8cf92e9-3d02-4765-a672-cedf1f5a2da3 35 fields · synced Jun 1, 2026