gudid
Primary ID: TW952-O
Leakbuster 3 (UDI TW952-O)
Manufactured by Starplex Scientific Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Leakbuster 3 - Primary ID TW952-O
Device Regulatory Overview
The Leakbuster 3 (Model/Catalog Number: TW952-O) is a medical device manufactured by Starplex Scientific Corp.. This product is indexed under FDA Product Code / Category Classification FMH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TW952-O
- Product Code / EMDN
- FMH
- Device Name
- Specimen Container, 90 ml, Tamper Evident Orange Cap, Individually Packaged in Peel Pack with Castile Soap Towelette, Sterile.
- Database Sync Date
- 2026-08-09 09:14:13
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 Leakbuster 3?
The registered manufacturer of record for Leakbuster 3 is Starplex Scientific Corp..
What is the Primary UDI-DI identifier for Leakbuster 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TW952-O.
What classification code is assigned to this device?
This device is registered under product classification code FMH.
Similar Classification Devices (FMH)
Other Devices by Starplex Scientific Corp.
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