← Back to catalogue

AROSmicro Suture Sterile

FDA UDI

Class II (US FDA UDI)

by Aros Surgical Instruments Corporation

Identity

Trade Name
AROSmicro Suture Sterile FDA UDI
Generic Name
Vascular clamp, single-use FDA UDI
Device Name
AROSuture-Sterile 9-0, 100 Microns, MET Point, 3/8 circle, 5 inches, 5mm, Box/12 FDA UDI
Model / Reference
T5A09N10 FDA UDI
Description
AROSuture-Sterile 9-0, 100 Microns, MET Point, 3/8 circle, 5 inches, 5mm, Box/12 FDA UDI

Identifiers

Catalog Number
T5A09N10 FDA UDI
Primary DI / UDI-DI
10818245020250 FDA UDI
FDA Product Code
GAR FDA UDI
GMDN Term
Vascular clamp, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5020 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vascular clamp, single-use

AROSmicro Suture Sterile by Aros Surgical Instruments Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular clamp, 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
Aros Surgical Instruments Corporation

Sources (1)

  • FDA UDI f7b6417c-dda2-404c-a29c-04349e761d47 36 fields · synced May 30, 2026