FDA UDI In Commercial Distribution 🇺🇸 United States

Prontosan®

DI: 04046964678233 · Model: 400518 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Prontosan®
Primary DI
04046964678233
Version / Model
400518
Catalog Number
400518
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
bdd105d9-ad06-4b1b-bae9-39112bfe4c8e

Device Description

Prontosan® Wound Gel X, 250g Tube

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRO Dressing, wound, drug

GMDN Terms

Code Name
59522 Wound hydrogel dressing, antimicrobial

Identifiers

Type ID
Primary 04046964678233
Unit of Use 04046964678226

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Weight : 250.000 G