Pmi

FDA UDI

Class I (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name: PMI FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: PMI Insufflation Tubing 10ft, .01 Micron Filter with Funnel Connector FDA UDI
Model / Reference: PMI-6000 FDA UDI
Description: PMI Insufflation Tubing 10ft, .01 Micron Filter with Funnel Connector FDA UDI

Identifiers

Catalog Number: PMI-6000 FDA UDI
Primary DI / UDI-DI: 00812608020171 FDA UDI
FDA Product Code: NKC FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.1730 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

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

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MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Progressive Medical, Inc.

Sources (1)

FDA UDI 38d391cf-b2ae-42c1-bc8a-fced75f5a7e2 34 fields · synced Jun 1, 2026