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Pmi

FDA UDI

Class II (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Vascular port administration set FDA UDI
Device Name
PMI Huber Safety Infusion Set 22G x 1” Needle, 6" tubing FDA UDI
Model / Reference
PMI221S FDA UDI
Description
PMI Huber Safety Infusion Set 22G x 1” Needle, 6" tubing FDA UDI

Identifiers

Catalog Number
PMI221S FDA UDI
Primary DI / UDI-DI
00812608021130 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Vascular port administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

No

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: Vascular port administration set

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

Similar devices

Also classified as Vascular port administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3575d5b2-115a-4bea-ac78-692dba33c69b 35 fields · synced May 30, 2026