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Scissor

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
SCISSOR FDA UDI
Generic Name
Ophthalmic surgical instrument handle, pneumatic FDA UDI
Device Name
CASTROVIEJO SCISSOR CVD SHARP SATIN 4" FDA UDI
Model / Reference
CASTROVIEJO SCISSOR FDA UDI
Description
CASTROVIEJO SCISSOR CVD SHARP SATIN 4" FDA UDI

Identifiers

Catalog Number
503655 FDA UDI
Primary DI / UDI-DI
B9745036550 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Ophthalmic surgical instrument handle, pneumatic 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI

Category: Ophthalmic surgical instrument handle, pneumatic

Scissor by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical instrument handle, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 883afe5d-a401-4914-bedd-c57b5dc57550 35 fields · synced Jun 6, 2026