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Diamatrix Ltd.

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix Ltd. FDA UDI
Generic Name
Suturing needle holder, single-use FDA UDI
Device Name
Barraquer Needle Holder, Fine Delicate Curved 10mm Smooth Jaws, Locking, Titanium FDA UDI
Model / Reference
N10-CLT FDA UDI
Description
Barraquer Needle Holder, Fine Delicate Curved 10mm Smooth Jaws, Locking, Titanium FDA UDI

Identifiers

Catalog Number
N10-CLT FDA UDI
Primary DI / UDI-DI
00810163790041 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Suturing needle holder, 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing needle holder, single-use

Diamatrix Ltd. by Diamatrix — 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

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI b2f1148f-f363-485b-b8cd-cb8f3cbace8d 34 fields · synced May 31, 2026