Heka Dur Soft (UDI 08715886007129)
Manufactured by Allion BV h.o.d.n. van Heek Medical
Device Regulatory Overview
The Heka Dur Soft (Model/Catalog Number: WI0168) is a medical device manufactured by Allion BV h.o.d.n. van Heek Medical. This product is indexed under FDA Product Code / Category Classification M0304010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WI0168
- Product Code / EMDN
- M0304010103
- Device Name
- Bandages
- Database Sync Date
- 2026-08-09 16:48:11
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 Heka Dur Soft?
The registered manufacturer of record for Heka Dur Soft is Allion BV h.o.d.n. van Heek Medical.
What is the Primary UDI-DI identifier for Heka Dur Soft?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08715886007129.
What classification code is assigned to this device?
This device is registered under product classification code M0304010103.
Similar Classification Devices (M0304010103)
Other Devices by Allion BV h.o.d.n. van Heek Medical
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