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Ophthalmic Electric Table

FDA UDI

Class I (US FDA UDI)

by Mdt Sp Z O O

Identity

Trade Name
Ophthalmic Electric Table FDA UDI
Generic Name
Ophthalmic instrument table, line-powered FDA UDI
Model / Reference
TT2C-1000 FDA UDI

Identifiers

Primary DI / UDI-DI
05907642694350 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

Ophthalmic Electric Table by Mdt Sp Z O O — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic instrument table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mdt Sp Z O O

Sources (1)

  • FDA UDI 482ce942-17e9-4da1-947e-09d64f7e4795 32 fields · synced Jun 8, 2026