← Back to catalogue
Advincula Delineator™ Uterine Manipulator
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref LH-SCOLPO-SMLModel AD750-KES25
Identity
- Trade Name
- Hoyte Sacrocolpopexy Tip FDA UDI
- Generic Name
- Uterine manipulator, single-use FDA UDI
- Device Name
- Advincula Delineator™ Uterine Manipulator EUDAMEDHoyte Sacrocolpopexy Tip- Small FDA UDI
- Model / Reference
- AD750-KES25 EUDAMEDLH-SCOLPO-SML EUDAMEDFDA UDI
- Description
- Hoyte Sacrocolpopexy Tip- Small FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937015256 EUDAMEDFDA UDI
- Basic UDI-DI
- 0888937TD015sYH EUDAMED
- FDA Product Code
- HDL FDA UDI
- EMDN Code
- U99 DEVICES FOR UROGENITAL SYSTEM - OTHER EUDAMED
- GMDN Term
- Uterine manipulator, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 884.4520 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Advincula Delineator™ Uterine Manipulator by CooperSurgical, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0888937TD015sYH | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CooperSurgical, Inc.
- EUDAMED SRN
- US-MF-000002607
- Authorised Representative
- CooperSurgical Distribution B.V. NL-AR-000000059
Sources (2)
- EUDAMED cca495f3-c5ac-4b8a-828e-b6d186d90237 61 fields · synced Jul 18, 2026
- FDA UDI ba697604-a964-4b6d-947c-f21ad9978a3d 33 fields · synced May 30, 2026