| Primary Device ID | 00887761995888 |
| NIH Device Record Key | e0a6c658-b020-4052-a3c6-8a06a5b4babd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | iLED |
| Version Model Number | 4068120 |
| 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 | 00887761995888 [Primary] |
| FTD | Lamp, surgical |
| 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 |