Primary Device ID | 00842071136475 |
NIH Device Record Key | 83b4957e-10fe-40ec-88d0-39b4a2239f9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AMT Guidewire |
Version Model Number | E4-GW-1 |
Catalog Number | E4-GW-1, 4-GW-1 |
Company DUNS | 038101861 |
Company Name | APPLIED MEDICAL TECHNOLOGY, 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 | 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 | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net | |
Phone | (440) 717-4000 |
cs@appliedmedical.net |
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 | 00842071136420 [Primary] |
GS1 | 00842071136475 [Package] Contains: 00842071136420 Package: Box (4-GW-1) [5 Units] In Commercial Distribution |
KNT | Tubes, Gastrointestinal (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-26 |
Device Publish Date | 2024-08-16 |
00842071111823 | Guidewire (.038"Dia x180cm, pouched) |
00842071106942 | Guidewire (.038"Dia x 90cm, pouched) |
00842071106928 | Guidewire (.018"Dia x 70cm, pouched) |
00842071130633 | Guidewire (.018"Dia x 45cm, pouched) |
00842071136512 | 0.038"Dia x 180cm Guidewire (Pouched), MDR |
00842071136505 | 0.038"Dia x 90cm Guidewire (Pouched), MDR |
00842071136499 | 0.038" Dia x 45cm Guidewire (Pouched), MDR |
00842071136482 | 0.018" Dia x 70cm Guidewire (Pouched), MDR |
00842071136475 | 0.018" Dia x 45cm Guidewire (Pouched), MDR |