gudid
Primary ID: 16000
ANAEROBIC JAR ASSEMBLY (UDI 16000)
Manufactured by HAGER WORLDWIDE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ANAEROBIC JAR ASSEMBLY - Primary ID 16000
Device Regulatory Overview
The ANAEROBIC JAR ASSEMBLY (Model/Catalog Number: 16000) is a medical device manufactured by HAGER WORLDWIDE, INC.. This product is indexed under FDA Product Code / Category Classification JTM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16000
- Product Code / EMDN
- JTM
- Device Name
- ANAEROBIC JAR ASSEMBLY
- Database Sync Date
- 2026-08-09 09:03:10
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 ANAEROBIC JAR ASSEMBLY?
The registered manufacturer of record for ANAEROBIC JAR ASSEMBLY is HAGER WORLDWIDE, INC..
What is the Primary UDI-DI identifier for ANAEROBIC JAR ASSEMBLY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16000.
What classification code is assigned to this device?
This device is registered under product classification code JTM.
Similar Classification Devices (JTM)
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