Primary Device ID | 07612449140426 |
NIH Device Record Key | 7fbd6ead-3dd1-4466-ba13-088fdcaa1f78 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prontosan® |
Version Model Number | 3908438 |
Catalog Number | 3908438 |
Company DUNS | 002397347 |
Company Name | B. BRAUN MEDICAL INC. |
Device Count | 10 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07612449140402 [Unit of Use] |
GS1 | 07612449140419 [Primary] |
GS1 | 07612449140426 [Package] Contains: 07612449140419 Package: Carton [16 Units] In Commercial Distribution |
FRO | Dressing, wound, drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-04 |
Device Publish Date | 2020-04-24 |
04046964295881 | Prontosan® Wound Gel, 30 mL Bottl e |
04046964295782 | Prontosan® Wound Irrigation Solut ion, 350 mL Bottle |
04046964295744 | Prontosan® Wound Irrigation Solut ion, 40 mL Ampule |
07612449140426 | PRONTOSAN WOUND IRRIGATION CAP "USA" |
04046964295843 | PRONTOSAN WOUND IRRIGATION SOLUT. 1000ML |
04046964678233 | Prontosan® Wound Gel X, 250g Tube |
04046955726479 | PRONTOSAN SOLUTION RF "US" 350ML-STERIL |
04046955651092 | Prontosan® Wound Irrigation Solution, 1000 mL Bottle |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRONTOSAN 77349334 3652026 Live/Registered |
B. Braun Medical Inc. 2007-12-11 |