FDA UDI In Commercial Distribution 🇺🇸 United States

Perifix®

DI: 04046964183232 · Model: 415004 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Perifix®
Primary DI
04046964183232
Version / Model
415004
Catalog Number
415004
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2020-11-12
Public Version Status
Update
Public Device Record Key
2544f099-66e5-45b6-8546-86ed12c40c35

Device Description

PERIFIX® PinPad™ - securement device for PERIFIX 0.2 µm Flat Epidural Filter

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder

Identifiers

Type ID
Primary 04046964183232
Unit of Use 04046964183225

Customer Contacts