gudid
Primary ID: SA001020
HealiAid (UDI SA001020)
Manufactured by MAXIGEN BIOTECH INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HealiAid - Primary ID SA001020
Device Regulatory Overview
The HealiAid (Model/Catalog Number: SA001020) is a medical device manufactured by MAXIGEN BIOTECH INC.. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SA001020
- Product Code / EMDN
- KGN
- Device Name
- HealiAid collagen wound dressing is fabricated by native fibrous, absorbable type I collagen, purified from bovine Achilles tendons. HealiAid can greatly enchance and accelerate tissue ingrowth and support bone augmentation. SA001020 size: 10(dia) x 20mm
- Database Sync Date
- 2026-08-09 09:15:30
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 HealiAid?
The registered manufacturer of record for HealiAid is MAXIGEN BIOTECH INC..
What is the Primary UDI-DI identifier for HealiAid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SA001020.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by MAXIGEN BIOTECH INC.
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