FDA UDI In Commercial Distribution 🇺🇸 United States

ZAVATION

DI: 00842166117976 · Model: 97-4040 · ZAVATION LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZAVATION
Primary DI
00842166117976
Version / Model
97-4040
Catalog Number
NA
Company Name
ZAVATION LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-07
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b9cc4e64-5ca3-4013-a649-174f48d9f8b6

Device Description

Polyaxial Shaft Screw 4.0x40mm

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWP Appliance, Fixation, Spinal Interlaminal
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

Code Name
61306 Microplate seal roller IVD

Identifiers

Type ID
Primary 00842166117976

Customer Contacts

Phone
601-919-1119