eudamed_udi
Primary ID: 06438263665713
STERIKING® Pouches for robotic instruments (UDI 06438263665713)
Manufactured by Wipak Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERIKING® Pouches for robotic instruments - Primary ID 06438263665713
Device Regulatory Overview
The STERIKING® Pouches for robotic instruments (Model/Catalog Number: SdV20) is a medical device manufactured by Wipak Oy. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SdV20
- Product Code / EMDN
- S01010101
- Device Name
- STERIKING® Pouches and Rolls
- Database Sync Date
- 2026-08-09 16:29:57
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 STERIKING® Pouches for robotic instruments?
The registered manufacturer of record for STERIKING® Pouches for robotic instruments is Wipak Oy.
What is the Primary UDI-DI identifier for STERIKING® Pouches for robotic instruments?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438263665713.
What classification code is assigned to this device?
This device is registered under product classification code S01010101.
Similar Classification Devices (S01010101)
Other Devices by Wipak Oy
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