FDA UDI In Commercial Distribution 🇺🇸 United States

Vital™

DI: 00887868310201 · Model: 850M0077 · BIOMET SPINE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vital™
Primary DI
00887868310201
Version / Model
850M0077
Catalog Number
850M0077
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-29
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
47dc6efa-f6de-456c-98f5-34a48d157cb8

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
HXX Screwdriver

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00887868310201

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Vital™ MIS Reduction Driver