gudid
Primary ID: 1LICFNG-S
Intercept Free (UDI 1LICFNG-S)
Manufactured by P H & S PRODUCTS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Intercept Free - Primary ID 1LICFNG-S
Device Regulatory Overview
The Intercept Free (Model/Catalog Number: 1LICFNG-S) is a medical device manufactured by P H & S PRODUCTS LLC. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1LICFNG-S
- Product Code / EMDN
- QDO
- Device Name
- 8.25mil Fingertip, 12" in Length, Nitrile, NFPA Approved, Accelerator, Sulfur & Zinc Free, Powder Free, Textured Finger Tips, White/Green, Size Small
- Database Sync Date
- 2026-08-09 09:37:45
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 Intercept Free?
The registered manufacturer of record for Intercept Free is P H & S PRODUCTS LLC.
What is the Primary UDI-DI identifier for Intercept Free?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1LICFNG-S.
What classification code is assigned to this device?
This device is registered under product classification code QDO.
Similar Classification Devices (QDO)
Other Devices by P H & S PRODUCTS LLC
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