Primary Device ID | 00844505009874 |
NIH Device Record Key | 95d0da4d-2054-42b5-8378-8c05ae4c3b00 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DragonFly™ CHARGING SYSTEM |
Version Model Number | 950-005 |
Company DUNS | 030849173 |
Company Name | Grace Medical, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)472-2363 |
info@gracemedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00844505009874 [Primary] |
ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2018-09-22 |
00844505014403 - ApollOS | 2024-05-13 ApollOS™ |
10844505014394 - TOUMA VENT TUBE W/ TAB | 2024-01-31 MODIFIED TOUMA VENT TUBE W/ TAB 1.27MM ID SILICONE |
10844505014004 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 5 PACK |
10844505014042 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 5 PACK |
10844505014080 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 10 PACK |
10108445050141 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 10 PACK |
10844505014165 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 30 PACK |
10844505014189 - ARMSTRONG VENT TUBE | 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 30 PACK |