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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Medical/surgical interventional tube/cable securement clip, reusable FDA UDI
Device Name
Armstand FDA UDI
Model / Reference
ARMSTAND FDA UDI
Description
Armstand FDA UDI

Identifiers

Catalog Number
ARMSTAND FDA UDI
Primary DI / UDI-DI
30845854081215 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Medical/surgical interventional tube/cable securement clip, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

Category: Medical/surgical interventional tube/cable securement clip, reusable

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

Similar devices

Also classified as Medical/surgical interventional tube/cable securement clip, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 1df751b6-3f14-40b1-bbe3-18384f991192 35 fields · synced May 31, 2026