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Stradis

FDA UDI

Class I (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
STRADIS FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
STERILE SEPARATES CASTROVIEJO SCISSORS FDA UDI
Model / Reference
525-165 FDA UDI
Description
STERILE SEPARATES CASTROVIEJO SCISSORS FDA UDI

Identifiers

Primary DI / UDI-DI
M7525251651 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 11.5 Centimeter FDA UDI

Stradis by Stradis Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d35add1-5d5d-4335-87c9-56956d5d029d 36 fields · synced May 31, 2026