Primary Device ID | 00821925030831 |
NIH Device Record Key | 5b53a04d-5fca-4a38-95d4-742d8c97bdd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gyrus ACMI |
Version Model Number | 7089-0856 |
Company DUNS | 007198742 |
Company Name | Gyrus ACMI, LLC |
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 | 00821925030831 [Package] Contains: 00821925034662 Package: [10 Units] In Commercial Distribution |
GS1 | 00821925034662 [Primary] |
EMX | Balloon, Epistaxis |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-04 |
Device Publish Date | 2024-11-26 |
00821925017979 | STRAIGHT VENT TUBE FLPL .045", TWIN PACK (60/PK) |
00821925037908 | Gauze Sack and O-Ring (10/PK) |
00821925030831 | Blu Epistaxis Pack, Large 10.0 cm x 1.5 cm x 2.5 cm, Bacteriostatic (10/PK) |
00821925027329 | E-Z GRIP GUIDEWIRE TORQUE DEVICE (5/PK) |
00821925036147 | 5 FR Open End Ureteral Catheter 5.0 FR (1.667 mm) X 70 cm (10/PK) |
00821925002630 | Fluid Pouch Disposable (12/PK) |
00821925007932 | Replacement Knob Assembly (4/PK) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GYRUS ACMI 78845492 3410751 Live/Registered |
GYRUS ACMI, INC. 2006-03-24 |