gudid
Primary ID: 1600766
PM2-A150 (UDI 1600766)
Manufactured by Bien-Air Surgery SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PM2-A150 - Primary ID 1600766
Device Regulatory Overview
The PM2-A150 (Model/Catalog Number: 1600766) is a medical device manufactured by Bien-Air Surgery SA. This product is indexed under FDA Product Code / Category Classification HBE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1600766
- Product Code / EMDN
- HBE
- Device Name
- Database Sync Date
- 2026-08-09 09:03:20
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 PM2-A150?
The registered manufacturer of record for PM2-A150 is Bien-Air Surgery SA.
What is the Primary UDI-DI identifier for PM2-A150?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1600766.
What classification code is assigned to this device?
This device is registered under product classification code HBE.
Similar Classification Devices (HBE)
Other Devices by Bien-Air Surgery SA
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