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Contrast Injection Line

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Contrast Injection Line FDA UDI
Generic Name
Radiographic procedure tubing FDA UDI
Device Name
Contrast Injection Line 48" (122cm) M/F (PVC) 1000 PSI FDA UDI
Model / Reference
197248 FDA UDI
Description
Contrast Injection Line 48" (122cm) M/F (PVC) 1000 PSI FDA UDI

Identifiers

Catalog Number
197248 FDA UDI
Primary DI / UDI-DI
00886333208678 FDA UDI
510(k) Number
K963749 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Radiographic procedure tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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: Radiographic procedure tubing

Contrast Injection Line by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiographic procedure tubing.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 88ee1d6f-737e-4f6d-9769-023b39f833b6 37 fields · synced Jun 9, 2026