Primary Device ID | 00303620000109 |
NIH Device Record Key | 622fd8a5-abe2-459b-a5c7-de51b1cc9ada |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 2 INCH CLEAR CONT NYL FILM (0002) |
Version Model Number | 01I0002 |
Company DUNS | 012925513 |
Company Name | SEPTODONT, 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 | false |
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 | false |
OTC Over-The-Counter | false |
Phone | (303) 665-7535 |
usregulatoryaffairs@septodont.com |
Width | 2 Inch |
Storage Environment Temperature | Between 59 Degrees Fahrenheit and 86 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00303620000109 [Primary] |
FRG | Wrap, Sterilization |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-09-12 |
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00303620000109 - 2 INCH CLEAR CONT NYL FILM (0002) | 2019-11-082 INCH CLEAR CONT NYL FILM (0002) |
00303620000109 - 2 INCH CLEAR CONT NYL FILM (0002) | 2019-11-08 2 INCH CLEAR CONT NYL FILM (0002) |
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