gudid
Primary ID: 26413BN
EXEL HYPO NDL 22GX1-1/4" BULK, N-S (UDI 26413BN)
Manufactured by Exel International
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXEL HYPO NDL 22GX1-1/4" BULK, N-S - Primary ID 26413BN
Device Regulatory Overview
The EXEL HYPO NDL 22GX1-1/4" BULK, N-S (Model/Catalog Number: 26413BN) is a medical device manufactured by Exel International. This product is indexed under FDA Product Code / Category Classification FMF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 26413BN
- Product Code / EMDN
- FMF
- Device Name
- EXEL HYPO NDL 22GX1-1/4" BULK, N-S 20,000/CRTN
- Database Sync Date
- 2026-08-09 09:00:33
Full Regulatory Attributes
🔒 Token Gated
{
"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 EXEL HYPO NDL 22GX1-1/4" BULK, N-S?
The registered manufacturer of record for EXEL HYPO NDL 22GX1-1/4" BULK, N-S is Exel International.
What is the Primary UDI-DI identifier for EXEL HYPO NDL 22GX1-1/4" BULK, N-S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26413BN.
What classification code is assigned to this device?
This device is registered under product classification code FMF.
Similar Classification Devices (FMF)
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