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Malosa Medical

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Malosa Medical FDA UDI
Generic Name
Eye spud FDA UDI
Device Name
Golf Club Spud FDA UDI
Model / Reference
MMSU1417S FDA UDI
Description
Golf Club Spud FDA UDI

Identifiers

Catalog Number
MMSU1417S FDA UDI
Primary DI / UDI-DI
35055186223763 FDA UDI
FDA Product Code
HNA FDA UDI
GMDN Term
Eye spud FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

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

Category: Eye spud

Malosa Medical by Beaver-Visitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye spud.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 65c051e2-36b2-4510-9f00-f3728eb6bc31 35 fields · synced May 30, 2026