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Pmi

FDA UDI

Class I (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Interventional radiology percutaneous-access kit, single-use FDA UDI
Device Name
PMI Combo Pack Includes: Disposable Lap Cholangiography Catheter (PMIXL11) FDA UDI
Model / Reference
PMIXLPIN FDA UDI
Description
PMI Combo Pack Includes: Disposable Lap Cholangiography Catheter (PMIXL11) FDA UDI

Identifiers

Catalog Number
PMIXLPIN FDA UDI
Primary DI / UDI-DI
00812608020997 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
Interventional radiology percutaneous-access kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa6db473-9b5d-484f-8325-d305df48d20b 36 fields · synced May 30, 2026