Primary Device ID | 00084424900337 |
NIH Device Record Key | 6b7c47ba-ef51-4dc9-ba61-db7fa3c2127b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hospitak, Mouth to Mask Resuscitator Adult Medium Mask |
Version Model Number | 1058-E |
Catalog Number | 1058-E |
Company DUNS | 809784593 |
Company Name | CONVATEC, PURCHASING DEPARTMENT |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00084424900337 [Primary] |
GS1 | 20844249003330 [Package] Package: case [20 Units] In Commercial Distribution |
BTM | Ventilator, Emergency, Manual (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-01 |
Device Publish Date | 2015-10-15 |
10768455203946 - ESTEEM | 2024-09-23 N/A |
10768455209481 - ESENTA | 2024-09-03 ESENTA THIN XL SEMI CIRCLE (1X20PK) EUR |
10768455209511 - ESENTA | 2024-09-03 ESENTA THIN CURVE 3X9CM (1X80PK) NAI |
00768455204793 - GENTLECATH | 2024-04-15 GENTLECATH AIR FEM V2.0 CH10 1X30PK US |
00768455204823 - GENTLECATH | 2024-04-15 GENTLECATH AIR FEM V2.0 CH12 1X30PK US |
00768455204854 - GENTLECATH | 2024-04-15 GENTLECATH AIR FEM V2.0 CH14 1X30PK US |
00768455207145 - GENTLECATH | 2024-04-15 GENTLECATH AIR FEM V2.0 CH10 1X10PK US |
00768455207169 - GENTLECATH | 2024-04-15 GENTLECATH AIR FEM V2.0 CH12 1X10PK US |