← Back to catalogue

25ga DEX Stiff Curved Horizontal Scissors

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
25ga DEX Stiff Curved Horizontal Scissors FDA UDI
Generic Name
Intraocular scissors, probe-like, single-use FDA UDI
Model / Reference
DVS5006-25-S FDA UDI

Identifiers

Primary DI / UDI-DI
10840096205180 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, probe-like, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraocular scissors, probe-like, single-use

25ga DEX Stiff Curved Horizontal Scissors by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors, probe-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a37483b3-3d4e-45be-b2c1-be080a6b200c 32 fields · synced Jun 7, 2026