Primary Device ID | 00867622000456 |
NIH Device Record Key | c748f9dd-c1da-4ac2-a6c6-c4b105aea00e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | bFed™ |
Version Model Number | SK-2002 |
Catalog Number | SK-2002 |
Company DUNS | 080494259 |
Company Name | U DELIVER MEDICAL L.L.C. |
Device Count | 40 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00867622000456 [Primary] |
GS1 | 00867622000470 [Unit of Use] |
PIF | Gastrointestinal Tubes With Enteral Specific Connectors |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-05-03 |
Device Publish Date | 2018-02-02 |
00867622000456 | bFed Refill kit containing 10 Large Cap Bolink™ Gravity Feeding Sets with ENFit® Connector ( |
00867622000449 | bFed Starter kit containing 5 Large Cap Bolink™ Gravity Feeding Sets with ENFit® Connector ( |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BFED 88649828 not registered Live/Pending |
U Deliver Medical 2019-10-10 |