Primary Device ID | 05019778006607 |
NIH Device Record Key | d245f4d1-7e5a-49b6-84e6-1b4a4fbd9d96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Olumpus |
Version Model Number | TC-C4 |
Company DUNS | 217061423 |
Company Name | KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT) LIMITED |
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 | 05019778006607 [Direct Marking] |
GS1 | 15019778006604 [Primary] |
FEM | Accessories, Photographic, For Endoscope (Exclude Light Sources) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-02 |
Device Publish Date | 2019-09-24 |
05019778008656 - Olympus | 2023-11-07 |
05019778008663 - Olympus | 2023-11-07 |
05019778008670 - Olympus | 2023-11-07 |
05019778008687 - Olympus | 2023-11-07 |
15019778007700 - Olympus | 2023-07-26 |
15019778007717 - Olympus | 2023-07-26 |
15019778007724 - Olympus | 2023-07-26 |
15019778007731 - Olympus | 2023-07-26 |