Primary Device ID | 20858835007046 |
NIH Device Record Key | 8eb3a264-f9dd-4dee-9e53-7ef9dc7e076b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biotronix Healthcare |
Version Model Number | GE36412 |
Catalog Number | GE36412 |
Company DUNS | 065762392 |
Company Name | BIOTRONIX HEALTHCARE INDUSTRIES, INC. |
Device Count | 1 |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00858835007042 [Primary] |
GS1 | 10858835007049 [Package] Contains: 00858835007042 Package: Inner Box [100 Units] In Commercial Distribution |
GS1 | 20858835007046 [Package] Contains: 10858835007049 Package: Case [100 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-12-24 |
Device Publish Date | 2019-10-06 |
20858835007053 | Disposable Hypodermic Needles 23G x 1" |
20858835007046 | Disposable Hypodermic Needles 22G x 1 1/2" |
20858835007039 | Disposable Hypodermic Needle 21G x 1 1/2 |
20858835007022 | Disposable Hypodermic Needle 20G x 1 1/2" |
20858835007015 | Disposable Hypodermic Needle 18G x 1 1/2" |
20858835007008 | Disposable Hypodermic Needles 18G x 1" |
10850005165283 | Enteral Delivery Gravity Bag Set w/ ENFit™* Connector |
10850005165276 | Enteral Delivery Pump Bag Set w/ ENFit™* Connector |
10850005165108 | Nebulizer with Pediatric Elongated Mask, 7ft. No Crush Tubing and Standard Connector |
10850005165092 | Nebulizer with Adult Mask, 7ft. No Crush Tubing and Standard Connector |
10850005165078 | Nebulizer with Elongated Adult Mask, 7ft. No Crush Tubing and Universal Connector |
10850005165054 | Minor Laceration Tray w/ Instrument |
10850005165047 | Irrigation Tray with Piston Syringe |
10850005165030 | Irrigation Tray with Bulb Syringe |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOTRONIX HEALTHCARE 86094840 4616297 Live/Registered |
Biotronix Healthcare Industries Inc. 2013-10-18 |