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Endosee

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Endosee FDA UDI
Generic Name
Flexible fibreoptic hysteroscope FDA UDI
Device Name
Endosee System Convenience Kit with IV Tube Instrument Tray for Hysteroscopy FDA UDI
Model / Reference
ES-TRAY-IV FDA UDI
Description
Endosee System Convenience Kit with IV Tube Instrument Tray for Hysteroscopy FDA UDI

Identifiers

Primary DI / UDI-DI
60888937026674 FDA UDI
FDA Product Code
FAJ FDA UDI
HIH FDA UDI
GMDN Term
Flexible fibreoptic hysteroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
884.1690 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

Yes

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

Category: Flexible fibreoptic hysteroscope

Endosee by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible fibreoptic hysteroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d5fcb86-c4d0-498c-a9e3-892859875ef1 33 fields · synced Jun 9, 2026