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Pmi

FDA UDI

Class II (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Laparoscope system, reusable FDA UDI
Device Name
PMI Cholangiogram Grasper Stainless Steel Replacement Cap - Reusable FDA UDI
Model / Reference
PMI790-SCREW FDA UDI
Description
PMI Cholangiogram Grasper Stainless Steel Replacement Cap - Reusable FDA UDI

Identifiers

Catalog Number
PMI790-SCREW FDA UDI
Primary DI / UDI-DI
00812608021581 FDA UDI
FDA Product Code
GCL FDA UDI
GMDN Term
Laparoscope system, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Laparoscope system, reusable

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

Similar devices

Also classified as Laparoscope system, reusable.

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 502b8ca0-1483-4d1c-bdc0-459c34320ea9 35 fields · synced May 30, 2026