eudamed_udi
Primary ID: 04719878041461
SterileRight (UDI 04719878041461)
Manufactured by SterileRight Packaging Mfg.Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SterileRight - Primary ID 04719878041461
Device Regulatory Overview
The SterileRight (Model/Catalog Number: P101.01.5803) is a medical device manufactured by SterileRight Packaging Mfg.Inc.. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P101.01.5803
- Product Code / EMDN
- S01020201
- Device Name
- Sterilization Tyvek Flat Rolls
- Database Sync Date
- 2026-08-09 16:28:46
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 SterileRight?
The registered manufacturer of record for SterileRight is SterileRight Packaging Mfg.Inc..
What is the Primary UDI-DI identifier for SterileRight?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719878041461.
What classification code is assigned to this device?
This device is registered under product classification code S01020201.
Similar Classification Devices (S01020201)
Other Devices by SterileRight Packaging Mfg.Inc.
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