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Minerva Desiccant

FDA UDI

Class III (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name
Minerva Desiccant FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument FDA UDI
Device Name
Minerva Desiccant FDA UDI
Model / Reference
MINDESI FDA UDI
Description
Minerva Desiccant FDA UDI

Identifiers

Catalog Number
MINDESI FDA UDI
Primary DI / UDI-DI
00862393000155 FDA UDI
FDA Product Code
MNB FDA UDI
GMDN Term
Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

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

Minerva Desiccant by Minerva Surgical, Inc. — Class III — 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 0d1dfd97-7f1c-4def-83bc-1338b4947353 35 fields · synced May 30, 2026