← Back to catalogue

Sklar Instruments

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar Instruments FDA UDI
Generic Name
Suturing needle holder, single-use FDA UDI
Device Name
ECONO STERILE WEBSTER NH FINE 5.25" STER 25 FDA UDI
Model / Reference
96-2740A FDA UDI
Description
ECONO STERILE WEBSTER NH FINE 5.25" STER 25 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111488276 FDA UDI
FDA Product Code
HXK FDA UDI
GMDN Term
Suturing needle holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Suturing needle holder, single-use

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

Similar devices

Also classified as Suturing needle holder, 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 fb9107b4-c652-4a9b-973b-f54acfeb881a 33 fields · synced Jun 1, 2026