FDA UDI In Commercial Distribution 🇺🇸 United States

VFT

DI: 03662663035880 · Model: VF9165R · LDR Spine Usa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VFT
Primary DI
03662663035880
Version / Model
VF9165R
Catalog Number
VF9165R
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
6
Public Version Date
2022-11-07
Public Version Status
Update
Public Device Record Key
00fb7c40-2fd3-498c-8e21-86a52216b5cd

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
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 03662663035880

Customer Contacts

Phone
800-699-3360

Device Sizes

Type Value Unit Text
Height 58 Millimeter