Primary Device ID | 14048223018597 |
NIH Device Record Key | c05697cb-3b80-40c7-a05b-ff0b9cb7d14d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EpiLong II |
Version Model Number | 0621152-51 |
Catalog Number | 0621152-51 |
Company DUNS | 317654283 |
Company Name | Pajunk GmbH Medizintechnologie |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com | |
Phone | +1(888)972-5865 |
info@pajunk-usa.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048223018590 [Unit of Use] |
GS1 | 14048223018597 [Primary] |
CAZ | Anesthesia conduction kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-09-05 |
14048223018597 | EpiLong II Tuohy 18G x 90mm, 20G x 90cm Cat |
04048223119501 | EpiLong II Tuohy II needle 18G x 90mm, with plastic stylet |