gudid
Primary ID: 1.13.12
BEAR (UDI 1.13.12)
Manufactured by Mytamed, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BEAR - Primary ID 1.13.12
Device Regulatory Overview
The BEAR (Model/Catalog Number: 1.13.12) is a medical device manufactured by Mytamed, Inc.. This product is indexed under FDA Product Code / Category Classification JZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.13.12
- Product Code / EMDN
- JZF
- Device Name
- Frazier-Ferguson Suction, 12 Fr
- Database Sync Date
- 2026-08-09 09:04:03
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 BEAR?
The registered manufacturer of record for BEAR is Mytamed, Inc..
What is the Primary UDI-DI identifier for BEAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.13.12.
What classification code is assigned to this device?
This device is registered under product classification code JZF.
Similar Classification Devices (JZF)
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