GUDIDData
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gudid Primary ID: 48 012

N/A (UDI 48 012)

Manufactured by SALTER LABS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 48 012

Device Regulatory Overview

The N/A (Model/Catalog Number: 48 012) is a medical device manufactured by SALTER LABS. This product is indexed under FDA Product Code / Category Classification EJL within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 2 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1898-2012 View Full Alert →

Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use ...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-0360-2014 View Full Alert →

Salter Labs EtCO2 Sample line 15' (4.6 M) tube, male luer connectors. Rx only; Made in Mexico; Manufacturer:Salter Labs, 100 West Sycamore ...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
48 012
Product Code / EMDN
EJL
Device Name
Adult. EtCO2 Oral/Nasal Sampling Cannula, male slip tip connector
Database Sync Date
2026-08-09 09:01:02

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of N/A?

The registered manufacturer of record for N/A is SALTER LABS.

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48 012.

What classification code is assigned to this device?

This device is registered under product classification code EJL.

Similar Classification Devices (EJL)

Other Devices by SALTER LABS

Programmatic Export

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