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Novaplus®

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Novaplus® FDA UDI
Generic Name
Circumcision kit, single-use FDA UDI
Device Name
Kit: Circumcision NOVAPLUS 20/Cs FDA UDI
Model / Reference
56631 FDA UDI
Description
Kit: Circumcision NOVAPLUS 20/Cs FDA UDI

Identifiers

Primary DI / UDI-DI
10809160005675 FDA UDI
FDA Product Code
OHG FDA UDI
GMDN Term
Circumcision kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: Circumcision kit, single-use

Novaplus® by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Circumcision kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Action Industries Inc.

Sources (1)

  • FDA UDI ab1b7c8c-db99-47ec-8199-1953614a0806 34 fields · synced May 30, 2026