Genesys HTA Scope Adapter, OLYMPUS

FDA UDI

Class I (US FDA UDI)

by Minerva Surgical, Inc.

Identity

Trade Name: Genesys HTA Scope Adapter, OLYMPUS FDA UDI
Generic Name: Endoscope sheath, reusable FDA UDI
Device Name: OLYMPUS Scope Adapter, for use only with Genesys HTA System FDA UDI
Model / Reference: M006550360 FDA UDI
Description: OLYMPUS Scope Adapter, for use only with Genesys HTA System FDA UDI

Identifiers

Catalog Number: M006550360 FDA UDI
Primary DI / UDI-DI: 00850033976199 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope sheath, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Minerva Surgical, Inc.

Sources (1)

FDA UDI fbd377f1-0b08-41f9-8ea1-9d231a307aac 35 fields · synced Jun 1, 2026