eudamed_udi
Primary ID: 04710810119279
CV-3 Manifold (UDI 04710810119279)
Manufactured by GaleMed Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CV-3 Manifold - Primary ID 04710810119279
Device Regulatory Overview
The CV-3 Manifold (Model/Catalog Number: AV0006) is a medical device manufactured by GaleMed Corporation. This product is indexed under FDA Product Code / Category Classification R02010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AV0006
- Product Code / EMDN
- R02010101
- Device Name
- Manifold
- Database Sync Date
- 2026-08-09 16:29:08
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 CV-3 Manifold?
The registered manufacturer of record for CV-3 Manifold is GaleMed Corporation.
What is the Primary UDI-DI identifier for CV-3 Manifold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710810119279.
What classification code is assigned to this device?
This device is registered under product classification code R02010101.
Similar Classification Devices (R02010101)
- → BREATHING CIRCUITS, W/O WATER TRAP
- → Vital Signs™ Breathing Circuit, Pediatric, Disposable, 1.8 m/72 in
- → Vital Signsâ„¢ Breathing Circuit, Pediatric, Corrugated, Disposable, 2.4m / 96in, With Gas Sampling Straight Connector, HMEF Mini, Manual Bag 1L, Manual Ventilation Tube, Corrugated, 1.5 M, Gas Sampling Line, 3 mÂ
- → ALTECH
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