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Argyle

FDA UDI

Class II (US FDA UDI)

by Mozarc Medical US LLC

Identity

Trade Name
Argyle FDA UDI
Generic Name
Catheter injection port FDA UDI
Device Name
Chronic Catheter Accessory,Injection Sealing Cap FDA UDI
Model / Reference
8813791001 FDA UDI
Description
Chronic Catheter Accessory,Injection Sealing Cap FDA UDI

Identifiers

Primary DI / UDI-DI
30884521003945 FDA UDI
510(k) Number
K844193 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Catheter injection port FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

No

FDA UDI

Category: Catheter injection port

Argyle by Mozarc Medical US LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catheter injection port.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c21b3c22-132c-4c39-a9a9-7e4bcfa6c311 35 fields · synced Jun 8, 2026