gudid
Primary ID: 209-00-47
AWI (UDI 209-00-47)
Manufactured by Apex (Suzhou) Medical Products Company
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AWI - Primary ID 209-00-47
Device Regulatory Overview
The AWI (Model/Catalog Number: 209-00-47) is a medical device manufactured by Apex (Suzhou) Medical Products Company. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 209-00-47
- Product Code / EMDN
- FQH
- Device Name
- Tunnel Tip
- Database Sync Date
- 2026-08-09 09:05:24
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 AWI?
The registered manufacturer of record for AWI is Apex (Suzhou) Medical Products Company.
What is the Primary UDI-DI identifier for AWI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 209-00-47.
What classification code is assigned to this device?
This device is registered under product classification code FQH.
Similar Classification Devices (FQH)
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