gudid
Primary ID: 72936000
Multipac patient pack (UDI 72936000)
Manufactured by Intersurgical Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Multipac patient pack - Primary ID 72936000
Device Regulatory Overview
The Multipac patient pack (Model/Catalog Number: 72936000) is a medical device manufactured by Intersurgical Incorporated. This product is indexed under FDA Product Code / Category Classification OFP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 72936000
- Product Code / EMDN
- OFP
- Device Name
- Multipac patient pack (includes 1 Filta-Therm HMEF 1941000, 1 anesthesia mask elbow and 1 ClearLite size 3 - anesthetic face mask 7293000)
- Database Sync Date
- 2026-08-09 09:31:32
Full Regulatory Attributes
🔒 Token Gated
{
"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 Multipac patient pack?
The registered manufacturer of record for Multipac patient pack is Intersurgical Incorporated.
What is the Primary UDI-DI identifier for Multipac patient pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 72936000.
What classification code is assigned to this device?
This device is registered under product classification code OFP.
Similar Classification Devices (OFP)
Other Devices by Intersurgical Incorporated
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