Sampler, Amniotic Fluid (Amniocentesis Tray) (UDI HIO)
Device Regulatory Overview
The Sampler, Amniotic Fluid (Amniocentesis Tray) (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification HIO within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- HIO
- Device Name
- Sampler, Amniotic Fluid (Amniocentesis Tray)
- Database Sync Date
- 2026-08-09 09:00:27
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 Sampler, Amniotic Fluid (Amniocentesis Tray)?
The registered manufacturer of record for Sampler, Amniotic Fluid (Amniocentesis Tray) is .
What is the Primary UDI-DI identifier for Sampler, Amniotic Fluid (Amniocentesis Tray)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HIO.
What classification code is assigned to this device?
This device is registered under product classification code HIO.
Similar Classification Devices (HIO)
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