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Gass Corneoscleral Punch

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
GASS CORNEOSCLERAL PUNCH FDA UDI
Generic Name
Corneoscleral punch FDA UDI
Device Name
GASS CORNEOSCLERAL PUNCH ROTATABLE TIP DEEP BITE FDA UDI
Model / Reference
11-9200 FDA UDI
Description
GASS CORNEOSCLERAL PUNCH ROTATABLE TIP DEEP BITE FDA UDI

Identifiers

Catalog Number
11-9200 FDA UDI
Primary DI / UDI-DI
00192896012752 FDA UDI
FDA Product Code
HNJ FDA UDI
GMDN Term
Corneoscleral punch 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

Dimensions & Sizes

Size
Outer Diameter — 1 Millimeter FDA UDI

Category: Corneoscleral punch

Gass Corneoscleral Punch by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneoscleral punch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 21f7b2c2-7f70-4ef8-a255-56975a8f8483 36 fields · synced May 29, 2026