Primary Device ID | 04048551317488 |
NIH Device Record Key | c5df8104-ec53-4f9c-b52c-cdf8526d7007 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | n.a |
Version Model Number | 20161220 |
Catalog Number | 20161220 |
Company DUNS | 315731430 |
Company Name | Karl Storz GmbH & Co. KG |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048551317488 [Primary] |
NTN | Led light source |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-09 |
Device Publish Date | 2024-11-29 |
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04048551012468 - NA | 2025-04-07 Irrigation Tube, for cleaning |
04048551061343 - NA | 2025-04-07 15 Touch Screen |
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04048551069493 - NA | 2025-04-07 Mandrin, for 204808 |
04048551069530 - NA | 2025-04-07 Mandrin, for 204809 |