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Nanoduct® Electrode Cable Set Assembly

FDA UDI

Class II (US FDA UDI)

by Elitechgroup Inc.

Identity

Trade Name
Nanoduct® Electrode Cable Set Assembly FDA UDI
Generic Name
Sweat-induction iontophoresis device/conductivity analyser FDA UDI
Device Name
For use with Nanoduct Neonatal Sweat Analysis System to induce sweat for diagnosis of Cystic Fibrosis. FDA UDI
Model / Reference
RP-359 FDA UDI
Description
For use with Nanoduct Neonatal Sweat Analysis System to induce sweat for diagnosis of Cystic Fibrosis. FDA UDI

Identifiers

Primary DI / UDI-DI
03661540302022 FDA UDI
510(k) Number
K010031 FDA UDI
FDA Product Code
KTB FDA UDI
GMDN Term
Sweat-induction iontophoresis device/conductivity analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5525 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sweat-induction iontophoresis device/conductivity analyser

Nanoduct® Electrode Cable Set Assembly by Elitechgroup Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sweat-induction iontophoresis device/conductivity analyser.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elitechgroup Inc.

Sources (1)

  • FDA UDI eab95ecc-cad8-4170-8b42-a9b8138205c7 35 fields · synced May 31, 2026