gudid
Primary ID: 50502
LEISEGANG (UDI 50502)
Manufactured by Coopersurgical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LEISEGANG - Primary ID 50502
Device Regulatory Overview
The LEISEGANG (Model/Catalog Number: 50502) is a medical device manufactured by Coopersurgical, Inc.. This product is indexed under FDA Product Code / Category Classification GEH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 50502
- Product Code / EMDN
- GEH
- Device Name
- LM-900 CO2 Cryosurgery System. Contents: 1 Cryogun, replacement O-rings, cleaning plugs and gas scavenging hose.
- Database Sync Date
- 2026-08-09 09:16:47
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 LEISEGANG?
The registered manufacturer of record for LEISEGANG is Coopersurgical, Inc..
What is the Primary UDI-DI identifier for LEISEGANG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50502.
What classification code is assigned to this device?
This device is registered under product classification code GEH.
Similar Classification Devices (GEH)
Other Devices by Coopersurgical, Inc.
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