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Dhaliwal Scleral Buckle Crescent Blade, Straight

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Dhaliwal Scleral Buckle Crescent Blade, Straight FDA UDI
Generic Name
Ophthalmic knife, reusable FDA UDI
Device Name
Dhaliwal Scleral Buckle Crescent Blade, Straight FDA UDI
Model / Reference
VG7965-S275 FDA UDI
Description
Dhaliwal Scleral Buckle Crescent Blade, Straight FDA UDI

Identifiers

Primary DI / UDI-DI
00840096210927 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Ophthalmic knife, 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

Category: Ophthalmic knife, reusable

Dhaliwal Scleral Buckle Crescent Blade, Straight by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic knife, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1126a76c-bd2e-433c-b9eb-5a1b5f5fca07 33 fields · synced May 31, 2026