W 613 / DORSI-FLEXION BANDAGE PLUS (LOW-FOOT)(UNIVERSAL) (UDI 08681190364824)
Manufactured by Doğam Medikal Kozmetik LTD. STI.
Device Regulatory Overview
The W 613 / DORSI-FLEXION BANDAGE PLUS (LOW-FOOT)(UNIVERSAL) (Model/Catalog Number: W 613) is a medical device manufactured by Doğam Medikal Kozmetik LTD. STI.. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W 613
- Product Code / EMDN
- Y061218
- Device Name
- ANKLE SUPPORTS, WALKERS, WEIGHTS
- Database Sync Date
- 2026-08-09 16:30:13
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 W 613 / DORSI-FLEXION BANDAGE PLUS (LOW-FOOT)(UNIVERSAL)?
The registered manufacturer of record for W 613 / DORSI-FLEXION BANDAGE PLUS (LOW-FOOT)(UNIVERSAL) is Doğam Medikal Kozmetik LTD. STI..
What is the Primary UDI-DI identifier for W 613 / DORSI-FLEXION BANDAGE PLUS (LOW-FOOT)(UNIVERSAL)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681190364824.
What classification code is assigned to this device?
This device is registered under product classification code Y061218.
Similar Classification Devices (Y061218)
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