Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in) (UDI 10705037016099)
Manufactured by Advanced Sterilization Products, Inc.
Device Regulatory Overview
The Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in) (Model/Catalog Number: 13834) is a medical device manufactured by Advanced Sterilization Products, Inc.. This product is indexed under FDA Product Code / Category Classification S010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13834
- Product Code / EMDN
- S010401
- Device Name
- APTIMAX™ Instrument Trays
- Database Sync Date
- 2026-08-09 16:29:50
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 Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in)?
The registered manufacturer of record for Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in) is Advanced Sterilization Products, Inc..
What is the Primary UDI-DI identifier for Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705037016099.
What classification code is assigned to this device?
This device is registered under product classification code S010401.
Similar Classification Devices (S010401)
Other Devices by Advanced Sterilization Products, Inc.
- → Aptimax™ Instrument Tray 380 mm x 250 mm x 30 mm (15 in x 10 in x 1.2 in)
- → Tyvek® Self Seal Pouch with STERRAD™ Chemical Indicator 250 mm x 480 mm (10" x 19")
- → Tyvek® Roll with STERRAD™ Chemical Indicator 500 mm x 70 m (20" x 76 yds.)
- → Tyvek® Roll with STERRAD™ Chemical Indicator 250 mm x 70 m (10" x 76 yds.)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint