gudid
Primary ID: M7008
ASEPT Peritoneal Drainage System (UDI M7008)
Manufactured by PFM MEDICAL INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASEPT Peritoneal Drainage System - Primary ID M7008
Device Regulatory Overview
The ASEPT Peritoneal Drainage System (Model/Catalog Number: M7008) is a medical device manufactured by PFM MEDICAL INCORPORATED. This product is indexed under FDA Product Code / Category Classification PNG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M7008
- Product Code / EMDN
- PNG
- Device Name
- ASEPT Peritoneal Drainage System
- Database Sync Date
- 2026-08-09 09:43:35
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 ASEPT Peritoneal Drainage System?
The registered manufacturer of record for ASEPT Peritoneal Drainage System is PFM MEDICAL INCORPORATED.
What is the Primary UDI-DI identifier for ASEPT Peritoneal Drainage System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M7008.
What classification code is assigned to this device?
This device is registered under product classification code PNG.
Similar Classification Devices (PNG)
Other Devices by PFM MEDICAL INCORPORATED
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