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Brachial/Axillary/Cerebral Drape

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Brachial/Axillary/Cerebral Drape FDA UDI
Generic Name
Angiographic drape FDA UDI
Device Name
Brachial/Axillary/Cerebral Drape 38 1/2" x 60" FDA UDI
Model / Reference
396204 FDA UDI
Description
Brachial/Axillary/Cerebral Drape 38 1/2" x 60" FDA UDI

Identifiers

Catalog Number
396204 FDA UDI
Primary DI / UDI-DI
00886333212491 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Angiographic drape FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Angiographic drape

Brachial/Axillary/Cerebral Drape by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic drape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argon Medical Devices, Inc.

Sources (1)

  • FDA UDI cb5b9f13-7dbb-4d68-ac15-e03bfafe5a19 36 fields · synced Jun 9, 2026