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Marco

FDA UDI

Class I (US FDA UDI)

by Takagi Seiko Co., Ltd.

Identity

Trade Name
MARCO FDA UDI
Generic Name
Ophthalmic slit lamp, surgical FDA UDI
Model / Reference
MARCO SURGISCOPE 3 FDA UDI

Identifiers

Primary DI / UDI-DI
04560323648601 FDA UDI
FDA Product Code
HRM FDA UDI
GMDN Term
Ophthalmic slit lamp, surgical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic slit lamp, surgical

Marco by Takagi Seiko Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic slit lamp, surgical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4e83f87c-1fe9-49b5-8b0b-52ea14d03719 32 fields · synced May 31, 2026