FDA UDI In Commercial Distribution 🇺🇸 United States

Stimuplex® Ultra 360®

DI: 04046964726590 · Model: 333646 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Stimuplex® Ultra 360®
Primary DI
04046964726590
Version / Model
333646
Catalog Number
333646
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
2019-04-29
Public Version Status
Update
Public Device Record Key
d24038a1-551d-437a-bdb6-75df252a488e

Device Description

Stimuplex® Ultra 360® 20 Ga. x 6 in. (150 mm) Insulated Echogenic Needle with 30° Bevel and Extension Set (STIMU320150)

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
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
45178 Peripheral nerve-block blunt needle

Identifiers

Type ID
Primary 04046964726590
Unit of Use 04046964726583

Customer Contacts