FDA UDI In Commercial Distribution 🇺🇸 United States

Stimuplex®

DI: 04022495101211 · Model: 4894260 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
Stimuplex®
Primary DI
04022495101211
Version / Model
4894260
Catalog Number
4894260
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
3
Public Version Date
2018-10-01
Public Version Status
Update
Public Device Record Key
53e81b9d-b9b5-43e2-ab2b-fb8edef355f7

Device Description

Stimuplex® A, 30° bevel (4894260)

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
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
BXN STIMULATOR, NERVE, BATTERY-POWERED

GMDN Terms

Code Name
45178 Peripheral nerve-block blunt needle

Identifiers

Type ID
Primary 04022495101211
Unit of Use 04022495101204

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Gauge (cannula) : 21