DUALSAN MONOCOLLANT TERAPEUTICO KKL1 DX - TG 04 (UDI 08054382242147)
Manufactured by Dual Sanitaly S.p.A. SB
Device Regulatory Overview
The DUALSAN MONOCOLLANT TERAPEUTICO KKL1 DX - TG 04 (Model/Catalog Number: 5D2515X00HI04) is a medical device manufactured by Dual Sanitaly S.p.A. SB. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5D2515X00HI04
- Product Code / EMDN
- Y061218
- Device Name
- DUALSAN MONOCOLLANT TERAPEUTICO a compressione decrescente KKL1 DX
- Database Sync Date
- 2026-08-09 16:29:03
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 DUALSAN MONOCOLLANT TERAPEUTICO KKL1 DX - TG 04?
The registered manufacturer of record for DUALSAN MONOCOLLANT TERAPEUTICO KKL1 DX - TG 04 is Dual Sanitaly S.p.A. SB.
What is the Primary UDI-DI identifier for DUALSAN MONOCOLLANT TERAPEUTICO KKL1 DX - TG 04?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054382242147.
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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