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Telemetry Totes

FDA UDI

Class I (US FDA UDI)

by Neotech Products LLC

Identity

Trade Name
Telemetry Totes FDA UDI
Generic Name
Personal device holder, single-use FDA UDI
Device Name
The Telemetry Totes are intended to hold a telemetry device. FDA UDI
Model / Reference
Valu-Tote FDA UDI
Description
The Telemetry Totes are intended to hold a telemetry device. FDA UDI

Identifiers

Catalog Number
A507 FDA UDI
Primary DI / UDI-DI
10812594011969 FDA UDI
FDA Product Code
JAY FDA UDI
GMDN Term
Personal device holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5280 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal device holder, single-use

Telemetry Totes by Neotech Products LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Personal device holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb7a411a-4fea-49bc-b034-994cd1890062 34 fields · synced Jun 6, 2026