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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
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
L-SHAPE HOOK ELECTRODE 5MM 32CM FDA UDI
Model / Reference
PMI-PMI5220582 FDA UDI
Description
L-SHAPE HOOK ELECTRODE 5MM 32CM FDA UDI

Identifiers

Catalog Number
PMI-PMI5220582 FDA UDI
Primary DI / UDI-DI
00850011214121 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, bipolar, 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: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, 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 50ace6d5-389a-4c4b-bfdd-6a4d650c2673 35 fields · synced May 29, 2026