gudid
Primary ID: W-18
LapPakOR (UDI W-18)
Manufactured by THE O R COMPANY PTY LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LapPakOR - Primary ID W-18
Device Regulatory Overview
The LapPakOR (Model/Catalog Number: W-18) is a medical device manufactured by THE O R COMPANY PTY LTD. This product is indexed under FDA Product Code / Category Classification GCZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W-18
- Product Code / EMDN
- GCZ
- Device Name
- Single piece bowel retractor
- Database Sync Date
- 2026-08-09 09:38:27
Full Regulatory Attributes
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{
"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 LapPakOR?
The registered manufacturer of record for LapPakOR is THE O R COMPANY PTY LTD.
What is the Primary UDI-DI identifier for LapPakOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W-18.
What classification code is assigned to this device?
This device is registered under product classification code GCZ.
Similar Classification Devices (GCZ)
Other Devices by THE O R COMPANY PTY LTD
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