eudamed_udi
Primary ID: 00197998040290
Solventum™ Transpore™ (UDI 00197998040290)
Manufactured by Solventum US LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solventum™ Transpore™ - Primary ID 00197998040290
Device Regulatory Overview
The Solventum™ Transpore™ (Model/Catalog Number: 1527-1S) is a medical device manufactured by Solventum US LLC. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1527-1S
- Product Code / EMDN
- M050101
- Device Name
- Solventum™ Transpore™ Surgical Tape
- Database Sync Date
- 2026-08-09 16:29:04
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 Solventum™ Transpore™?
The registered manufacturer of record for Solventum™ Transpore™ is Solventum US LLC.
What is the Primary UDI-DI identifier for Solventum™ Transpore™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00197998040290.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Solventum US LLC
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