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Vaginal Suppository Applicator

FDA UDI

Class I (US FDA UDI)

by Medisca Inc.

Identity

Trade Name
Vaginal Suppository Applicator FDA UDI
Generic Name
Vaginal applicator, single-use FDA UDI
Device Name
Vaginal Suppository Applicator FDA UDI
Model / Reference
9984-02 FDA UDI
Description
Vaginal Suppository Applicator FDA UDI

Identifiers

Catalog Number
9984-02 FDA UDI
Primary DI / UDI-DI
00338779998427 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

Vaginal Suppository Applicator by Medisca 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

Manufacturer
Medisca Inc.

Sources (1)

  • FDA UDI 643d0418-166e-4b13-95f7-f9f52ae60db0 34 fields · synced Jun 7, 2026