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Titanium Castroviejo Curved Corneal Scissors, Blunt Tips, Round Handle

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Titanium Castroviejo Curved Corneal Scissors, Blunt Tips, Round Handle FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Model / Reference
6007C-115 FDA UDI

Identifiers

Primary DI / UDI-DI
00840096202335 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, 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
MRI Safety
MR Conditional FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

Titanium Castroviejo Curved Corneal Scissors, Blunt Tips, Round Handle by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI f1c86fe0-f5c3-486a-940a-800e285f85a3 32 fields · synced May 30, 2026