FDA UDI In Commercial Distribution 🇺🇸 United States

VariLift-LX

DI: 00813210020191 · Model: CIE2-A013-C01 · Wenzel Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VariLift-LX
Primary DI
00813210020191
Version / Model
CIE2-A013-C01
Company Name
Wenzel Spine, Inc.
Labeler DUNS
832543255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
6
Public Version Date
2022-11-03
Public Version Status
Update
Public Device Record Key
e16a6e53-1697-4442-9120-9ae7880764e6

Device Description

13-15mm Inserter, with Distal Depth Marks

Device Characteristics

Single Use
No
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
Yes
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00813210020191

Customer Contacts

Phone
855-936-9351