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Genesys HTA Scope Adapter, WOLF

FDA UDI

Class I (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name
Genesys HTA Scope Adapter, WOLF FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
WOLF Scope Adapter, for use only with Genesys HTA System FDA UDI
Model / Reference
M006550340 FDA UDI
Description
WOLF Scope Adapter, for use only with Genesys HTA System FDA UDI

Identifiers

Catalog Number
M006550340 FDA UDI
Primary DI / UDI-DI
00850033976175 FDA UDI
FDA Product Code
NWW FDA UDI
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1690 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: Endoscope sheath, reusable

Genesys HTA Scope Adapter, WOLF by Minerva Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a6c485f-ea3e-4565-8302-c58903f1d6b6 35 fields · synced May 30, 2026