FDA UDI In Commercial Distribution 🇺🇸 United States

Zavation

DI: 00842166132276 · Model: 221-0607 · ZAVATION LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zavation
Primary DI
00842166132276
Version / Model
221-0607
Company Name
ZAVATION LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-02
Public Version
1
Public Version Date
2020-09-10
Public Version Status
New
Public Device Record Key
04088230-8930-4074-b0dc-dbb10694294c

Device Description

Ti3Z CIF 13mmx15mmx7mm -6 deg

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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00842166132276

Customer Contacts

Phone
601-919-1119