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Hyfrecator 2000

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
HYFRECATOR 2000 FDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Device Name
HYFRECATOR 2000 150VAC - 50/60 HZ FDA UDI
Model / Reference
7-900-115 FDA UDI
Description
HYFRECATOR 2000 150VAC - 50/60 HZ FDA UDI

Identifiers

Catalog Number
7-900-115 FDA UDI
Primary DI / UDI-DI
20653405031595 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical system generator 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical system generator

Hyfrecator 2000 by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI dfd6c7b4-d1c1-4815-9e6a-83619289dc2b 36 fields · synced May 30, 2026