Primary Device ID | 00812559010955 |
NIH Device Record Key | 7a562774-d349-49f8-81ac-aa24011cc937 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Model 30 Pneumatonometer |
Version Model Number | 16030 |
Company DUNS | 126650253 |
Company Name | REICHERT, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
OTC Over-The-Counter | false |
Phone | 1-888-849-8955 |
reichert.information@ametek.com | |
Phone | 1-888-849-8955 |
reichert.information@ametek.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812559010955 [Primary] |
HKX | Tonometer, Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-22 |
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00812559010962 | AC powered contact tonometer intended for the measurement of intraocular pressure (IOP). The de |
00812559010955 | AC powered contact tonometer intended for the measurement of intraocular pressure (IOP). The de |