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Pmi

FDA UDI

Class II (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
PMI Empty IV Bag 250mL; 2 ports FDA UDI
Model / Reference
PMI250ML FDA UDI
Description
PMI Empty IV Bag 250mL; 2 ports FDA UDI

Identifiers

Catalog Number
PMI250ML FDA UDI
Primary DI / UDI-DI
00812608021642 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 250 Milliliter FDA UDI

Category: Fluid transfer set, general-purpose

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

Similar devices

Also classified as Fluid transfer set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 35199611-b881-4bf0-ad6e-5984e24e183b 36 fields · synced May 30, 2026