gudid
Primary ID: PL240K
PermaLife (UDI PL240K)
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 PL240K
Device Regulatory Overview
The PermaLife (Model/Catalog Number: PL240K) 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
- PL240K
- Product Code / EMDN
- LPZ
- Device Name
- PermaLife Cell Culture Bag, 240ml, "K" Set
- 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 PL240K.
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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