gudid
Primary ID: ABTDUAW114704D
iScreen (UDI ABTDUAW114704D)
Manufactured by Instant Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iScreen - Primary ID ABTDUAW114704D
Device Regulatory Overview
The iScreen (Model/Catalog Number: ABTDUAW114704D) is a medical device manufactured by Instant Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification LCM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ABTDUAW114704D
- Product Code / EMDN
- LCM
- Device Name
- 14 Panel CLIA Waived Click Cup w/ SVTAMP1000, BAR300, BUP10, BZO300, COC300, MDMA500, MET1000, MTD300, OPI2000, OXY100, PCP25, PPX300, TCA1000, THC50 w/ SVT OX/SG/pH
- Database Sync Date
- 2026-08-09 09:31:19
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 iScreen?
The registered manufacturer of record for iScreen is Instant Technologies, Inc..
What is the Primary UDI-DI identifier for iScreen?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ABTDUAW114704D.
What classification code is assigned to this device?
This device is registered under product classification code LCM.
Similar Classification Devices (LCM)
Other Devices by Instant Technologies, Inc.
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