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Doselogix

FDA UDI

Class I (US FDA UDI)

by Team Technologies, Inc.

Identity

Trade Name
Doselogix FDA UDI
Generic Name
Vaginal applicator, single-use FDA UDI
Device Name
TCPERL01-ROSEQUARTZ, 35ML, PERL VAGINAL DOSING SYSTEM FDA UDI
Model / Reference
TCPERL01 FDA UDI
Description
TCPERL01-ROSEQUARTZ, 35ML, PERL VAGINAL DOSING SYSTEM FDA UDI

Identifiers

Catalog Number
755013 FDA UDI
Primary DI / UDI-DI
00813360022076 FDA UDI
FDA Product Code
HGD FDA UDI
GMDN Term
Vaginal applicator, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 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: Vaginal applicator, single-use

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

Similar devices

Also classified as Vaginal applicator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 768c6a8f-e83b-4685-a0f4-3cea158e39bb 35 fields · synced May 31, 2026