Primary Device ID | 25060112312667 |
NIH Device Record Key | fbeea2b2-3986-47f9-8d4b-2b0ee118d2e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LMA |
Version Model Number | IPN046543 |
Catalog Number | MT5060LYK2-CP |
Company DUNS | 002348191 |
Company Name | TELEFLEX INCORPORATED |
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 | true |
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(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060112312663 [Primary] |
GS1 | 25060112312667 [Package] Contains: 05060112312663 Package: Box [5 Units] In Commercial Distribution |
MEB | PUMP, INFUSION, ELASTOMERIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-16 |
25060112312384 | ARROW AutoFuser Disposable Pain Control Pump |
15060112313384 | LMA Supreme® Airway Plus Pack Size 2.5 |
15060112313377 | LMA Supreme® Airway Plus Pack Size 1.5 |
25060112313299 | Esophageal Intubation Detector - Bulb |
25060112313282 | Esophageal Intubation Detector - Syringe |
25060112313244 | Pediatric Laryngo-Tracheal Mucosal Atomization Device with 5ml Oral Syringe |
15060112313230 | Pediatric Laryngo-Tracheal Mucosal Atomization Device with 5ml Syringe |
25060112313220 | Pediatric Laryngo-Tracheal Mucosal Atomization Device without Syringe |
25060112313213 | Laringo-Tracheal Mucosal Atomatization Device without Syringe |
15060112313209 | Laringo-Tracheal Mucosal Atomatization Device without Syringe |
25060112313183 | Laringo-Tracheal Mucosal Atomatization Device with 5ml Oral Syringe |
25060112313176 | Laringo-Tracheal Mucosal Atomatization Device with 3ml Syringe |
25060112312902 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312896 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312889 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312872 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312865 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312858 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312841 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312834 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312827 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312803 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312797 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312780 | ARROW AutoSelector Disposable Pain Control Pump |
25060112312773 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312766 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312759 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312735 | ARROW AutoFuser Disposable Pain Control Pump |
15060112312714 | AF550x2ML/H 2ML-60LO FH 5" SAT C,4"IN |
25060112312704 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312674 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312667 | ARROW AutoFuser Disposable Pain Control Pump |
15060112312646 | AF 275 x 5ML/H 2ML-60LO FH 5"SAT C,4"IN |
15060112312639 | AF 275 x 5ML/H 2ML-60LO FH STD C,4"INAF |
25060112312629 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312612 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312582 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312544 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312537 | ARROW AutoFuser Disposable Pain Control Pump |
15060112312516 | AF 275x4ML/H 2ML-60LO FH 5" SAT C,4"IN |
15060112312509 | AF 275 x 4ML/H 2ML-60LO FH STD C,4"IN |
25060112312490 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312476 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312452 | ARROW AutoFuser Disposable Pain Control Pump |
25060112312445 | ARROW AutoFuser Disposable Pain Control Pump |
15060112312424 | AF 100x2ML/HR 2ML-60LO FH 5" SAT C,4" IN |
15060112312417 | AF 100 x 2ML/H 2ML-60LO FH STD C,4"IN |
15060112312363 | AF 275 x 2ML/H 2ML-60LO FH 5" SAT C,4"IN |
15060112312356 | AF 275 x 2ML/H 2ML-60LO FH STD C,4"IN |
25060112312322 | ARROW AutoFuser Disposable Pain Control Pump |