gudid
Primary ID: PL1000K
PermaLife Cell Culture Bag (UDI PL1000K)
Manufactured by ORIGEN BIOMEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PermaLife Cell Culture Bag - Primary ID PL1000K
Device Regulatory Overview
The PermaLife Cell Culture Bag (Model/Catalog Number: PL1000K) 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
- PL1000K
- Product Code / EMDN
- LPZ
- Device Name
- PermaLife Cell Culture Bag, 1000ml, "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 Cell Culture Bag?
The registered manufacturer of record for PermaLife Cell Culture Bag is ORIGEN BIOMEDICAL, INC..
What is the Primary UDI-DI identifier for PermaLife Cell Culture Bag?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PL1000K.
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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