gudid
Primary ID: CGD
CerviGrip Uterine Manipulator (UDI CGD)
Manufactured by SURGITOOLS PTY. LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CerviGrip Uterine Manipulator - Primary ID CGD
Device Regulatory Overview
The CerviGrip Uterine Manipulator (Model/Catalog Number: CGD) is a medical device manufactured by SURGITOOLS PTY. LTD.. This product is indexed under FDA Product Code / Category Classification HEW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CGD
- Product Code / EMDN
- HEW
- Device Name
- CerviGrip Uterine Manipulator blister pack containing 1 sterile unit
- Database Sync Date
- 2026-08-09 09:38:27
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CerviGrip Uterine Manipulator?
The registered manufacturer of record for CerviGrip Uterine Manipulator is SURGITOOLS PTY. LTD..
What is the Primary UDI-DI identifier for CerviGrip Uterine Manipulator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CGD.
What classification code is assigned to this device?
This device is registered under product classification code HEW.
Similar Classification Devices (HEW)
Other Devices by SURGITOOLS PTY. LTD.
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