Primary Device ID | 09351108000036 |
NIH Device Record Key | 95cbe982-2362-4031-9aa5-107db117f9d8 |
Commercial Distribution Discontinuation | 2050-10-25 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Circumplast |
Version Model Number | Circumplast 13mm |
Catalog Number | CIRC13MM |
Company DUNS | 226185194 |
Company Name | EMBOSS MEDICAL LIMITED |
Device Count | 25 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 09351108000036 [Primary] |
GS1 | 09351108000128 [Unit of Use] |
HFX | Clamp, Circumcision |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2016-10-25 |
09351108000074 | Circumplast 13mm Shipping Carton |
09351108000067 | Circumplast 12mm Shipping Carton |
09351108000050 | Circumplast 9.5mm Shipping Carton |
09351108000043 | Circumplast 11mm Shipping Carton |
09351108000036 | Circumplast single use infant male circumcision device, size 13mm |
09351108000029 | Circumplast single use infant male circumcision device, size 12mm |
09351108000012 | Circumplast single use infant male circumcision device, size 11mm |
09351108000005 | Circumplast single use infant male circumcision device, size 9.5mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CIRCUMPLAST 79129996 4545652 Live/Registered |
Novadien Healthcare Pty Ltd 2013-04-08 |