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Ecomed Angiographic

FDA UDI

Class II (US FDA UDI)

by Ecomed Solutions, LLC

Identity

Trade Name
Ecomed Angiographic FDA UDI
Generic Name
Angiography kit FDA UDI
Device Name
150mL Angiographic Syringe Kit Includes (1) fill straw FDA UDI
Model / Reference
128-100201 FDA UDI
Description
150mL Angiographic Syringe Kit Includes (1) fill straw FDA UDI

Identifiers

Catalog Number
128-100201 FDA UDI
Primary DI / UDI-DI
00855009006146 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiography kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Total Volume — 150 Milliliter FDA UDI

Category: Angiography kit

Ecomed Angiographic by Ecomed Solutions, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiography kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 300f71b7-a5a6-4c4e-b29d-8cf6a0df178c 37 fields · synced Jun 9, 2026