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Elmed

FDA UDI

Class II (US FDA UDI)

by Progressive Medical Instrumentation Inc

Identity

Trade Name
ELMED FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
HOOK BIOPSY PUNCH, 32CM 5MM FDA UDI
Model / Reference
PMI52-25571A1 FDA UDI
Description
HOOK BIOPSY PUNCH, 32CM 5MM FDA UDI

Identifiers

Catalog Number
PMI52-25571A1 FDA UDI
Primary DI / UDI-DI
00850011214381 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

Elmed by Progressive Medical Instrumentation Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Progressive Medical Instrumentation Inc

Sources (1)

  • FDA UDI 9f894a33-c7a3-4840-863a-4b2b16827a9c 35 fields · synced Jun 8, 2026