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Nanoduct® Electrode Strap, Medium, Qty 1

FDA UDI

Class II (US FDA UDI)

by Elitechgroup Inc.

Identity

Trade Name
Nanoduct® Electrode Strap, Medium, Qty 1 FDA UDI
Generic Name
Sweat-induction iontophoresis device/conductivity analyser FDA UDI
Device Name
For use with Neonatal Sweat Analysis System to attach electrodes and sensor cells used to induce and collect sweat for diagnosis of Cystic Fibrosis. FDA UDI
Model / Reference
RP-355 FDA UDI
Description
For use with Neonatal Sweat Analysis System to attach electrodes and sensor cells used to induce and collect sweat for diagnosis of Cystic Fibrosis. FDA UDI

Identifiers

Primary DI / UDI-DI
03661540301988 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 Strap, Medium, Qty 1 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 700c584b-fd61-4df1-9dbd-1fc009d6c808 35 fields · synced Jun 6, 2026