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Marco

FDA UDI

Class I (US FDA UDI)

by Blue.S4 Inc

Identity

Trade Name
Marco FDA UDI
Generic Name
Static ophthalmic equipment stand, manually-adjusted FDA UDI
Device Name
Marco Bravo 2 Stand - Model BR2-ST FDA UDI
Model / Reference
BR2-ST FDA UDI
Description
Marco Bravo 2 Stand - Model BR2-ST FDA UDI

Identifiers

Primary DI / UDI-DI
00628308210039 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Static ophthalmic equipment stand, manually-adjusted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Static ophthalmic equipment stand, manually-adjusted

Marco by Blue.S4 Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Static ophthalmic equipment stand, manually-adjusted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Blue.S4 Inc

Sources (1)

  • FDA UDI 9f8a8de4-3c5c-42f4-b5dd-95d0e134e7bb 33 fields · synced May 30, 2026