Primary Device ID | 00852683007292 |
NIH Device Record Key | 937d940c-0c55-431d-a8df-914fe4338423 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AIT-W2 |
Version Model Number | 25048-22-000 |
Company DUNS | 053547238 |
Company Name | TOPCON MEDICAL SYSTEMS, INC. |
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 | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00852683007292 [Primary] |
HRJ | Table, Instrument, Powered, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-05-25 |
Device Publish Date | 2022-12-07 |
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00852683007292 | AIT-W2 Adjustable Table 240 Volt; AC-Powered Ophthalmic Instrument Table |
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