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Greenwald Surgical Company, Inc.

FDA UDI

Class II (US FDA UDI)

by Grace Manufacturing Inc

Identity

Trade Name
Greenwald Surgical Company, Inc. FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, reprocessed FDA UDI
Device Name
Hurd Turbinate Electrode FDA UDI
Model / Reference
28230-00 FDA UDI
Description
Hurd Turbinate Electrode FDA UDI

Identifiers

Catalog Number
BT83 FDA UDI
Primary DI / UDI-DI
10801334000110 FDA UDI
FDA Product Code
HIN FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4150 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

No

FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, reprocessed

Greenwald Surgical Company, Inc. by Grace Manufacturing Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Manufacturing Inc

Sources (1)

  • FDA UDI f5c344b4-826d-49ed-ab9d-7ff4287ed240 34 fields · synced May 30, 2026