gudid
Primary ID: 1600331
OSSEODOC Control Unit + Pump (UDI 1600331)
Manufactured by Bien-Air Surgery SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OSSEODOC Control Unit + Pump - Primary ID 1600331
Device Regulatory Overview
The OSSEODOC Control Unit + Pump (Model/Catalog Number: 1600331) is a medical device manufactured by Bien-Air Surgery SA. This product is indexed under FDA Product Code / Category Classification ERL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1600331
- Product Code / EMDN
- ERL
- Device Name
- Database Sync Date
- 2026-08-09 09:09:45
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 OSSEODOC Control Unit + Pump?
The registered manufacturer of record for OSSEODOC Control Unit + Pump is Bien-Air Surgery SA.
What is the Primary UDI-DI identifier for OSSEODOC Control Unit + Pump?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1600331.
What classification code is assigned to this device?
This device is registered under product classification code ERL.
Similar Classification Devices (ERL)
Other Devices by Bien-Air Surgery SA
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