Primary Device ID | 00884838074262 |
NIH Device Record Key | 3cbc3046-f007-4a52-b869-0da11da27a94 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Height adjustable Trolley TA-M |
Version Model Number | 9890-010-87311 |
Catalog Number | 712031 |
Company DUNS | 314101218 |
Company Name | Philips Medical Systems DMC GmbH |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838074262 [Primary] |
IXR | Table, radiographic, tilting |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2016-09-19 |
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