FDA UDI In Commercial Distribution 🇺🇸 United States

NeoMagic

DI: B33920964000 · Model: 2096-400 · Neo Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NeoMagic
Primary DI
B33920964000
Version / Model
2096-400
Catalog Number
2096-400
Company Name
Neo Medical Inc.
Labeler DUNS
015510540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2025-07-22
Public Version Status
Update
Public Device Record Key
dc5c665b-4aa8-430e-a09c-a6c566f8c258

Device Description

1.9/2.0 Fr, 27ga, Needle & Tearaway Sheath Introducer

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Package B33920964005
Primary B33920964000

Customer Contacts

Phone
888-450-3334

Premarket Submissions

Submission Number Supplement Number
K983916 000

Device Sizes

Type Value Unit Text
Needle Gauge 27 Gauge
Catheter Gauge 1.9 French
Catheter Gauge 2.0 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Special Storage Condition, Specify
Special Conditions
Keep Away From Sunlight