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Stylus

FDA UDI

Class I (US FDA UDI)

by Surgical Specialties México, S. de R.L. de C.V.

Identity

Trade Name
Stylus FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
22.5DEG MICROSURGCL KNF STRAIGHT FDA UDI
Model / Reference
52-2201 FDA UDI
Description
22.5DEG MICROSURGCL KNF STRAIGHT FDA UDI

Identifiers

Catalog Number
52-2201 FDA UDI
Primary DI / UDI-DI
00848782025763 FDA UDI
FDA Product Code
EMF FDA UDI
GMDN Term
Manual scalpel blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual scalpel blade, single-use

Stylus by Surgical Specialties México, S. de R.L. de C.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 392b7735-3b40-4a1b-afb7-91108bd22bab 36 fields · synced May 30, 2026