Primary Device ID | 04056869961064 |
NIH Device Record Key | 232a8d43-329e-4215-a046-ab4850e34c62 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sparrow HP2 3 Ring |
Version Model Number | 10756474 |
Company DUNS | 868230876 |
Company Name | SIEMENS MEDICAL SOLUTIONS USA, 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 | 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 | 04056869961064 [Primary] |
KPS | System, tomography, computed, emission |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-08 |
Device Publish Date | 2024-01-31 |
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