← Back to catalogue

Sklar

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar FDA UDI
Generic Name
Dressing/utility forceps, tweezers-like, single-use FDA UDI
Device Name
ST MARTIN TY FCP 1X2 3.5CS/10 FDA UDI
Model / Reference
96-3632 FDA UDI
Description
ST MARTIN TY FCP 1X2 3.5CS/10 FDA UDI

Identifiers

Primary DI / UDI-DI
50649111456402 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Dressing/utility forceps, tweezers-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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dressing/utility forceps, tweezers-like, single-use

Sklar by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, tweezers-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

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 44ff3872-a198-483c-9d48-164af7d54a23 33 fields · synced May 30, 2026