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Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Barraquer Needle Holder, Extra Fine Jaws 8.00 mm, Curved, Without Lock, Small Size, Length 100 mm, Titanium FDA UDI
Model / Reference
8-025T FDA UDI
Description
Barraquer Needle Holder, Extra Fine Jaws 8.00 mm, Curved, Without Lock, Small Size, Length 100 mm, Titanium FDA UDI

Identifiers

Catalog Number
8-025T FDA UDI
Primary DI / UDI-DI
00840159902127 FDA UDI
FDA Product Code
FHQ FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suturing needle holder, reusable

Rumex by Rumex International Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8f124848-578d-4d04-9fdc-6fbe8b265878 34 fields · synced Jun 9, 2026