gudid
Primary ID: 7700OIN
BROSELOW (UDI 7700OIN)
Manufactured by VYAIRE MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BROSELOW - Primary ID 7700OIN
Device Regulatory Overview
The BROSELOW (Model/Catalog Number: 7700OIN) is a medical device manufactured by VYAIRE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification OKI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7700OIN
- Product Code / EMDN
- OKI
- Device Name
- INTUBATION MODULES
- Database Sync Date
- 2026-08-09 09:16:32
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BROSELOW?
The registered manufacturer of record for BROSELOW is VYAIRE MEDICAL, INC..
What is the Primary UDI-DI identifier for BROSELOW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7700OIN.
What classification code is assigned to this device?
This device is registered under product classification code OKI.
Similar Classification Devices (OKI)
Other Devices by VYAIRE MEDICAL, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint