gudid
Primary ID: M77460002
ASTOTUBE (UDI M77460002)
Manufactured by Stihler Electronic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASTOTUBE - Primary ID M77460002
Device Regulatory Overview
The ASTOTUBE (Model/Catalog Number: M77460002) is a medical device manufactured by Stihler Electronic GmbH. This product is indexed under FDA Product Code / Category Classification BSB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M77460002
- Product Code / EMDN
- BSB
- Device Name
- DEHP-free
- Database Sync Date
- 2026-08-09 09:17:36
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 ASTOTUBE?
The registered manufacturer of record for ASTOTUBE is Stihler Electronic GmbH.
What is the Primary UDI-DI identifier for ASTOTUBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M77460002.
What classification code is assigned to this device?
This device is registered under product classification code BSB.
Similar Classification Devices (BSB)
Other Devices by Stihler Electronic GmbH
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