Transanale Dekompressionssonde mit rektalem Ballon Set (TYP:AP NENNO) (UDI 04542187191042)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The Transanale Dekompressionssonde mit rektalem Ballon Set (TYP:AP NENNO) (Model/Catalog Number: 002-391-0220) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G0301010501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002-391-0220
- Product Code / EMDN
- G0301010501
- Device Name
- Transanal Ileus Decompression Tube Set
- Database Sync Date
- 2026-08-09 16:46:45
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 Transanale Dekompressionssonde mit rektalem Ballon Set (TYP:AP NENNO)?
The registered manufacturer of record for Transanale Dekompressionssonde mit rektalem Ballon Set (TYP:AP NENNO) is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for Transanale Dekompressionssonde mit rektalem Ballon Set (TYP:AP NENNO)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187191042.
What classification code is assigned to this device?
This device is registered under product classification code G0301010501.
Similar Classification Devices (G0301010501)
Other Devices by CREATE MEDIC CO., LTD.
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