← Back to catalogue

VCA Lite

FDA UDI

Class I (US FDA UDI)

by Pce, Inc.

Identity

Trade Name
VCA Lite FDA UDI
Generic Name
Vaginal applicator, single-use FDA UDI
Device Name
5.3 cc Vaginal Cream Applicator 3-Pack. Three applicators are packaged in a canister. FDA UDI
Model / Reference
Q033-G00-02 FDA UDI
Description
5.3 cc Vaginal Cream Applicator 3-Pack. Three applicators are packaged in a canister. FDA UDI

Identifiers

Primary DI / UDI-DI
00860009492912 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

Yes

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vaginal applicator, single-use

VCA Lite by Pce, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pce, Inc.

Sources (1)

  • FDA UDI 75a510d8-43a4-4069-9d61-65048f48c01b 33 fields · synced May 30, 2026