Primary Device ID | 00887761995871 |
NIH Device Record Key | 01c2f4c9-bda2-4365-a8f6-2a049d79dca6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | iLED |
Version Model Number | 4068130 |
Company DUNS | 330961223 |
Company Name | TRUMPF Medizin Systeme 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761995871 [Primary] |
FSQ | Light, surgical, instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-17 |
00887761995963 | Hospital Device |
00887761995956 | Hospital Device |
00887761995949 | Hospital Device |
00887761995888 | Hospital Device |
00887761995871 | Hospital Device |
00887761995864 | Hospital Device |
00887761995857 | Hospital Device |
00887761995840 | Hospital Device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ILED 87131140 5325155 Live/Registered |
Peter Sui Lun Fong 2016-08-08 |
ILED 85712308 not registered Dead/Abandoned |
McWong International, Inc. 2012-08-24 |
ILED 79023478 3202431 Live/Registered |
TRUMPF Medizin Systeme GmbH + Co. KG 2006-03-28 |
ILED 77302671 3599463 Dead/Cancelled |
Intematix Corporation 2007-10-12 |