Identity
- Trade Name
- Endosee FDA UDI
- Generic Name
- Flexible video hysteroscope FDA UDI
- Device Name
- Hysteroscope/Cystoscope, Charging Station, USB cable, and power cord FDA UDI
- Model / Reference
- OR-ES8000 FDA UDI
- Description
- Hysteroscope/Cystoscope, Charging Station, USB cable, and power cord FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937022452 FDA UDI
- 510(k) Number
- K170660 FDA UDI
- FDA Product Code
- FAJ FDA UDIHIH FDA UDI
- GMDN Term
- Flexible video hysteroscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI884.1690 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Flexible video hysteroscope
Endosee by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible video hysteroscope.
- VISERA HYSTEROVIDEOSCOPE — Olympus Medical Systems Corporation · Class II
- VISERA HYSTEROVIDEOSCOPE — Olympus Medical Systems Corporation · Class II
- Neoscope — Prosurg, Inc · Class II
- Endosee — CooperSurgical, Inc. · Class II
Cleared under the same submission
K170660 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 61f8afc0-c03d-4aa7-86ef-ca2b2efa70a2 34 fields · synced Jun 9, 2026