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Minerva Hegar Dilator (3 Pack)

FDA UDI

Class I (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name
Minerva Hegar Dilator (3 Pack) FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument FDA UDI
Device Name
Minerva Hegar Dilator (3 Pack) FDA UDI
Model / Reference
MIN8MM FDA UDI
Description
Minerva Hegar Dilator (3 Pack) FDA UDI

Identifiers

Catalog Number
MIN8MM FDA UDI
Primary DI / UDI-DI
00862393000179 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument

Minerva Hegar Dilator (3 Pack) by Minerva Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Minerva Surgical, Inc.

Sources (1)

  • FDA UDI b4448d7d-29fa-4d94-8d17-3565968f018f 35 fields · synced May 30, 2026