Ophthalmic Electric Table

GUDID 05907642694183

MDT SP Z O O

Ophthalmic instrument table, line-powered

• Primary Device ID: 05907642694183
• NIH Device Record Key: 1bb59ae5-272b-4b10-bc90-3402711f0717
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ophthalmic Electric Table
• Version Model Number: RT S
• Company DUNS: 366126408
• Company Name: MDT SP Z O O
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05907642694183 [Primary]

FDA Product Code

• HRJ: Table, Instrument, Powered, Ophthalmic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-24
• Device Publish Date: 2025-07-16

On-Brand Devices [Ophthalmic Electric Table]

• 05907642694107: MD-1
• 05907642694244: MD-X
• 05907642694350: TT2C-1000
• 05907642694343: TT2C-800
• 05907642694336: RT 2C
• 05907642694329: MD-3
• 05907642694312: MD-3V
• 05907642694305: TTVS-1000
• 05907642694299: RT V
• 05907642694282: TT-1060
• 05907642694275: MD-V
• 05907642694268: RT B
• 05907642694237: COMBO-2
• 05907642694220: RT VF
• 05907642694213: TTH-1000
• 05907642694206: MD-2
• 05907642694190: TT-4060
• 05907642694183: RT S
• 05907642694176: COMBO-1
• 05907642694169: TTUD-1000