eudamed_udi
Primary ID: 06923980106231
PEEP Valve, 5~20cmH2O, 22F (UDI 06923980106231)
Manufactured by GaleMed (Xiamen) Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEEP Valve, 5~20cmH2O, 22F - Primary ID 06923980106231
Device Regulatory Overview
The PEEP Valve, 5~20cmH2O, 22F (Model/Catalog Number: AV0038) is a medical device manufactured by GaleMed (Xiamen) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R030280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AV0038
- Product Code / EMDN
- R030280
- Device Name
- Disposable PEEP VALVE
- Database Sync Date
- 2026-08-09 18:26:37
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 PEEP Valve, 5~20cmH2O, 22F?
The registered manufacturer of record for PEEP Valve, 5~20cmH2O, 22F is GaleMed (Xiamen) Co., Ltd..
What is the Primary UDI-DI identifier for PEEP Valve, 5~20cmH2O, 22F?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06923980106231.
What classification code is assigned to this device?
This device is registered under product classification code R030280.
Similar Classification Devices (R030280)
Other Devices by GaleMed (Xiamen) Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint