Primary Device ID | 00809958088708 |
NIH Device Record Key | fbaad16f-6f0e-4a2b-9e44-d4531155e5dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bioguard Conforming Bandage |
Version Model Number | 97241 |
Catalog Number | 97241 |
Company DUNS | 200564891 |
Company Name | Derma Sciences Canada 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 | 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 | 00809958088708 [Primary] |
GS1 | 00809958088722 [Package] Package: corrugate box [100 Units] In Commercial Distribution |
NYS | Wound Dressing With Poly(Diallyl Dimethyl Ammonium Chloride)(Pdadmac) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2016-09-22 |
00809958088807 | Bioguard Conforming Bandage, 3 in x 4.1 yd (7.6 cm x 3.7 m), Stretched, 1 Roll |
00809958088708 | Bioguard Conforming Bandage, 2 in x 4.1 yd (5.1 cm x 3.7 cm), Stretched, 1 Roll |
00809958087305 | Bioguard Conforming Bandage, 4 in x 4.1 yd (10 cm x 3.7 m) Stretched, 1 Roll |