eudamed_udi
Primary ID: 06438263644114
STERIKING® LT-Blueline Heat-Sealable Rolls (UDI 06438263644114)
Manufactured by Wipak Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERIKING® LT-Blueline Heat-Sealable Rolls - Primary ID 06438263644114
Device Regulatory Overview
The STERIKING® LT-Blueline Heat-Sealable Rolls (Model/Catalog Number: LTR41A) is a medical device manufactured by Wipak Oy. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LTR41A
- Product Code / EMDN
- S01020201
- Device Name
- STERIKING® Pouches and Rolls
- Database Sync Date
- 2026-08-09 16:58:33
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® LT-Blueline Heat-Sealable Rolls?
The registered manufacturer of record for STERIKING® LT-Blueline Heat-Sealable Rolls is Wipak Oy.
What is the Primary UDI-DI identifier for STERIKING® LT-Blueline Heat-Sealable Rolls?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438263644114.
What classification code is assigned to this device?
This device is registered under product classification code S01020201.
Similar Classification Devices (S01020201)
Other Devices by Wipak Oy
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