eudamed_udi
Primary ID: 08435605805118
ESCOB.FLOCK NASOF. 80MM FLOW (UDI 08435605805118)
Manufactured by Deltalab, S.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ESCOB.FLOCK NASOF. 80MM FLOW - Primary ID 08435605805118
Device Regulatory Overview
The ESCOB.FLOCK NASOF. 80MM FLOW (Model/Catalog Number: 310217) is a medical device manufactured by Deltalab, S.L.. This product is indexed under FDA Product Code / Category Classification A1101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 310217
- Product Code / EMDN
- A1101
- Device Name
- ESCOBILLÓN FLOCADO DE NYLON ESTÉRIL CON SOPORTE DE ABS ROMPIBLE CON Y SIN MEDIO DE TRANSPORTE - STERILE FLOCKED NYLON SWAB WITH BREAKABLE ABS ROD WITH AND WITHOUT TRANSPORT MEDIUM
- Database Sync Date
- 2026-08-09 16:29:41
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 ESCOB.FLOCK NASOF. 80MM FLOW?
The registered manufacturer of record for ESCOB.FLOCK NASOF. 80MM FLOW is Deltalab, S.L..
What is the Primary UDI-DI identifier for ESCOB.FLOCK NASOF. 80MM FLOW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435605805118.
What classification code is assigned to this device?
This device is registered under product classification code A1101.
Similar Classification Devices (A1101)
Other Devices by Deltalab, S.L.
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