SENGSTAKEN TUBES (UDI G010201)
Device Regulatory Overview
The SENGSTAKEN TUBES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification G010201 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
- G010201
- Device Name
- SENGSTAKEN TUBES
- Database Sync Date
- 2026-08-09 16:18:37
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 SENGSTAKEN TUBES?
The registered manufacturer of record for SENGSTAKEN TUBES is .
What is the Primary UDI-DI identifier for SENGSTAKEN TUBES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G010201.
What classification code is assigned to this device?
This device is registered under product classification code G010201.
Similar Classification Devices (G010201)
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