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Crown Surgical

FDA UDI

Class I (US FDA UDI)

by Crown Surgical Corporation

Identity

Trade Name
CROWN SURGICAL FDA UDI
Generic Name
General-purpose surgical scissors, single-use FDA UDI
Device Name
IRIS Scissors, Straight, 4-1/2" PP BULK FDA UDI
Model / Reference
SCISSORS FDA UDI
Description
IRIS Scissors, Straight, 4-1/2" PP BULK FDA UDI

Identifiers

Catalog Number
11-138-PP FDA UDI
Primary DI / UDI-DI
B92411138PP0 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, single-use 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

Yes

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

No

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

Crown Surgical by Crown Surgical Corporation — 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

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Manufacturer

Manufacturer
Crown Surgical Corporation

Sources (1)

  • FDA UDI 2e4469fc-2db0-43ca-82b5-0a6114063364 35 fields · synced May 30, 2026