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Novaplus®

FDA UDI

Class I (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Novaplus® FDA UDI
Generic Name
Surgical sponge-counting rack FDA UDI
Device Name
Bag: Sponge Ct 10.25X32 2.0ml Blu 250/cs FDA UDI
Model / Reference
V3230 FDA UDI
Description
Bag: Sponge Ct 10.25X32 2.0ml Blu 250/cs FDA UDI

Identifiers

Primary DI / UDI-DI
20809160022204 FDA UDI
FDA Product Code
LWH FDA UDI
GMDN Term
Surgical sponge-counting rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2740 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical sponge-counting rack

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

Similar devices

Also classified as Surgical sponge-counting rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab9dd769-1546-4cd2-9e46-cae21c0fe4c9 34 fields · synced May 30, 2026