STERRAD™ Adaptor III (UDI 10705037016297)
Manufactured by Advanced Sterilization Products, Inc.
Device Regulatory Overview
The STERRAD™ Adaptor III (Model/Catalog Number: 15403) is a medical device manufactured by Advanced Sterilization Products, Inc.. This product is indexed under FDA Product Code / Category Classification S900103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 15403
- Product Code / EMDN
- S900103
- Device Name
- STERRAD™ Adaptor
- Database Sync Date
- 2026-08-09 16:59:22
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 STERRAD™ Adaptor III?
The registered manufacturer of record for STERRAD™ Adaptor III is Advanced Sterilization Products, Inc..
What is the Primary UDI-DI identifier for STERRAD™ Adaptor III?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705037016297.
What classification code is assigned to this device?
This device is registered under product classification code S900103.
Similar Classification Devices (S900103)
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")
- → Aptimax™ Instrument Tray 380 mm x 150 mm x 30 mm (15 in x 6 in x 1.2 in)
- → Tyvek® Roll with STERRAD™ Chemical Indicator 500 mm x 70 m (20" x 76 yds.)
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