FDA UDI In Commercial Distribution 🇺🇸 United States

VerteFIT

DI: 03662663033190 · Model: VF9108R · LDR Spine Usa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VerteFIT
Primary DI
03662663033190
Version / Model
VF9108R
Catalog Number
VF9108R
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-12
Public Version
5
Public Version Date
2025-01-03
Public Version Status
Update
Public Device Record Key
579a5c09-99a7-4c54-94f7-d541bc01ab59

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
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
MQP Spinal Vertebral Body Replacement Device

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 03662663033190

Customer Contacts

Phone
800-699-3360