gudid
Primary ID: PL70-2G
PermaLife (UDI PL70-2G)
Manufactured by ORIGEN BIOMEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PermaLife - Primary ID PL70-2G
Device Regulatory Overview
The PermaLife (Model/Catalog Number: PL70-2G) is a medical device manufactured by ORIGEN BIOMEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification LPZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PL70-2G
- Product Code / EMDN
- LPZ
- Device Name
- PermaLife cell culture bag, 70 ml, no green vent cap
- Database Sync Date
- 2026-08-09 09:46:38
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 PermaLife?
The registered manufacturer of record for PermaLife is ORIGEN BIOMEDICAL, INC..
What is the Primary UDI-DI identifier for PermaLife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PL70-2G.
What classification code is assigned to this device?
This device is registered under product classification code LPZ.
Similar Classification Devices (LPZ)
Other Devices by ORIGEN BIOMEDICAL, INC.
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