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Doselogix

FDA UDI

Class I (US FDA UDI)

by Team Technologies, Inc.

Identity

Trade Name
Doselogix FDA UDI
Generic Name
Medicine cup, single-use FDA UDI
Device Name
DOSELOGIX TC5-P-LIGHTSAFE 5 ML POINTED APPLICATOR FDA UDI
Model / Reference
TC5-P-LIGHTSAFE FDA UDI
Description
DOSELOGIX TC5-P-LIGHTSAFE 5 ML POINTED APPLICATOR FDA UDI

Identifiers

Catalog Number
755425 FDA UDI
Primary DI / UDI-DI
00813360022830 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Medicine cup, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Medicine cup, single-use

Doselogix by Team Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine cup, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Team Technologies, Inc.

Sources (1)

  • FDA UDI cdbfe7b0-4a22-4108-9c5f-209dc79205a1 35 fields · synced Jun 1, 2026