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Pmi

FDA UDI

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Peripheral intravenous catheterization support kit FDA UDI
Device Name
PMI IV START KIT W/CHLORAPREP LATEX FREE FDA UDI
Model / Reference
K703C FDA UDI
Description
PMI IV START KIT W/CHLORAPREP LATEX FREE FDA UDI

Identifiers

Catalog Number
K703C FDA UDI
Primary DI / UDI-DI
00812608021406 FDA UDI
GMDN Term
Peripheral intravenous catheterization support kit FDA UDI

Classification

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

No

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

Category: Peripheral intravenous catheterization support kit

Pmi by Progressive Medical, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous catheterization support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Progressive Medical, Inc.

Sources (1)

  • FDA UDI 254cc14b-67a1-4168-8d0d-245d7ae8fd47 35 fields · synced Jun 1, 2026