Primary Device ID | 04046955130061 |
NIH Device Record Key | 9bcb0346-61a1-4ab2-add2-84fb183fb648 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Contiplex® Ultra 360® |
Version Model Number | 339211 |
Catalog Number | 339211 |
Company DUNS | 002397347 |
Company Name | B. BRAUN MEDICAL INC. |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04046955130061 [Unit of Use] |
GS1 | 04046955130078 [Primary] |
CAZ | Anesthesia conduction kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-12 |
Device Publish Date | 2023-09-04 |
04046955130184 | CONTI TUOHY ULTRA 360 6" CONT PNB NRFIT |
04046955130160 | CONTI TUOHY ULTRA 360 4" CONT PNB NRFIT |
04046955130146 | CONTI TUOHY ULTRA 360 2" CONT PNB NRFIT |
04046955130245 | 18G x 4 CONT UTRA 360 20G EC CATH NRFIT |
04046955130061 | CONTI ECHO CT W/4" TUOHY ULTRA 360 NRFIT |
04046955130047 | CONTI ECHO CT W/2" TUOHY ULTRA 360 NRFIT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CONTIPLEX 86785264 4968600 Live/Registered |
B. BRAUN MELSUNGEN AG 2015-10-12 |
CONTIPLEX 73514624 1349123 Live/Registered |
B. BRAUN MELSUNGEN AG 1984-12-20 |