Primary Device ID | 04055207012918 |
NIH Device Record Key | b82cb873-8850-4cb5-97da-9efeeddd2e33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENDOLIGHT |
Version Model Number | 5160001 |
Catalog Number | 5160001 |
Company DUNS | 315304071 |
Company Name | Richard Wolf GmbH |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04055207012918 [Primary] |
NTN | Led light source |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2017-07-21 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ENDOLIGHT 75324963 not registered Dead/Abandoned |
ESC Medical Systems Ltd. 1997-07-15 |