gudid
Primary ID: 504555CHL
QUEST DIAGNOSTICS (UDI 504555CHL)
Manufactured by Asp Global, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QUEST DIAGNOSTICS - Primary ID 504555CHL
Device Regulatory Overview
The QUEST DIAGNOSTICS (Model/Catalog Number: 504555CHL) is a medical device manufactured by Asp Global, LLC. This product is indexed under FDA Product Code / Category Classification NNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 504555CHL
- Product Code / EMDN
- NNK
- Device Name
- SPECIMEN BAG 6.75" X 11" 2MIL PINK FILM FRONT, CLEAR BACK, 3 COLORS, 2MIL INNER POUCH, W/BARCODE, ZIP LOCK, 100/PK, 20PKS/CS, 2,000/CASE
- Database Sync Date
- 2026-08-09 09:12:13
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of QUEST DIAGNOSTICS?
The registered manufacturer of record for QUEST DIAGNOSTICS is Asp Global, LLC.
What is the Primary UDI-DI identifier for QUEST DIAGNOSTICS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 504555CHL.
What classification code is assigned to this device?
This device is registered under product classification code NNK.
Similar Classification Devices (NNK)
Other Devices by Asp Global, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint