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Gen2

FDA UDI

Class I (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
GEN2 FDA UDI
Generic Name
Corneal scissors, reusable FDA UDI
Device Name
CASTRO KERATOPLASTY SCISSORS BLUNT TIPS SMALL BLADES FDA UDI
Model / Reference
G2G36949 FDA UDI
Description
CASTRO KERATOPLASTY SCISSORS BLUNT TIPS SMALL BLADES FDA UDI

Identifiers

Catalog Number
G2G36949 FDA UDI
Primary DI / UDI-DI
00840343716219 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Corneal scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 5.25 Inch FDA UDI

Category: Corneal scissors, reusable

Gen2 by Surgix Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgix Medical Llc

Sources (1)

  • FDA UDI b2f68bb8-8456-4b9a-9569-f9d55cc54236 36 fields · synced Jun 1, 2026