FDA UDI In Commercial Distribution 🇺🇸 United States

INZONE

DI: 04546540697950 · Model: M00345100950 · Stryker Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INZONE
Primary DI
04546540697950
Version / Model
M00345100950
Catalog Number
451009-5
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-21
Public Version
7
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
fc125587-8e06-477a-a8d7-bd04d4d368d5

Device Description

DETACHMENT SYSTEM

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
KRD Device, Vascular, for Promoting Embolization
HCG DEVICE, NEUROVASCULAR EMBOLIZATION

GMDN Terms

Code Name
60637 Vascular implant detacher, electronic, single-use

Identifiers

Type ID
Primary 04546540697950

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dry, dark place.