FDA UDI In Commercial Distribution 🇺🇸 United States

Stimuplex®

DI: 04046964180101 · Model: 333576 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stimuplex®
Primary DI
04046964180101
Version / Model
333576
Catalog Number
333576
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-22
Public Version
4
Public Version Date
2020-03-03
Public Version Status
Update
Public Device Record Key
3d70e5d1-14bf-49aa-9edc-8f2bfd234560

Device Description

Stimuplex® HNS11/12 Replacement Cable (HEC)

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BXN STIMULATOR, NERVE, BATTERY-POWERED

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 04046964180101

Customer Contacts