gudid
Primary ID: MAJ-853
Biopsy Valve (UDI MAJ-853)
Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biopsy Valve - Primary ID MAJ-853
Device Regulatory Overview
The Biopsy Valve (Model/Catalog Number: MAJ-853) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification ODG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MAJ-853
- Product Code / EMDN
- ODG
- Device Name
- "MAJ-853 Biopsy valves 140-AL5/160-OL5"
- Database Sync Date
- 2026-08-09 09:46:01
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 Biopsy Valve?
The registered manufacturer of record for Biopsy Valve is OLYMPUS MEDICAL SYSTEMS CORP..
What is the Primary UDI-DI identifier for Biopsy Valve?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MAJ-853.
What classification code is assigned to this device?
This device is registered under product classification code ODG.
Similar Classification Devices (ODG)
Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.
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