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VISUCORE 500 Table

FDA UDIEUDAMED

Class I (US FDA UDI)

by Cx Engineering Sp Z O O

Identity

Trade Name
VISUCORE 500 Table FDA UDI
Generic Name
Ophthalmic instrument table, line-powered FDA UDI
Model / Reference
3 FDA UDI

Identifiers

Catalog Number
77230203 FDA UDI
Primary DI / UDI-DI
05904815700160 FDA UDI
FDA Product Code
HRJ FDA UDI
GMDN Term
Ophthalmic instrument table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4855 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

Yes

FDA UDI

Category: Ophthalmic instrument table, line-powered

VISUCORE 500 Table by Cx Engineering Sp Z O O — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic instrument table, line-powered.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 88669f40-7339-479a-aacb-80b4bdb2a737 33 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026