20 Microliter Pipette (UDI 00816068020597)
Manufactured by Advanced Instruments, LLC
Device Regulatory Overview
The 20 Microliter Pipette (Model/Catalog Number: 240820) is a medical device manufactured by Advanced Instruments, LLC. This product is indexed under FDA Product Code / Category Classification W0503020199 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses the method of freezing point depression to measure osmolality of serum...
GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Counter System is intended for use by trained healthcare professionals in cl...
Technical Specifications
- Model Number
- 240820
- Product Code / EMDN
- W0503020199
- Device Name
- Osmometer Accessories
- Database Sync Date
- 2026-08-09 16:51:06
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 20 Microliter Pipette?
The registered manufacturer of record for 20 Microliter Pipette is Advanced Instruments, LLC.
What is the Primary UDI-DI identifier for 20 Microliter Pipette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816068020597.
What classification code is assigned to this device?
This device is registered under product classification code W0503020199.
Similar Classification Devices (W0503020199)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint