FDA UDI In Commercial Distribution 🇺🇸 United States

VENTO XLPE Liner

DI: 03701089520232 · Model: 1-01-12-8656 · AMPLITUDE SAS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VENTO XLPE Liner
Primary DI
03701089520232
Version / Model
1-01-12-8656
Company Name
AMPLITUDE SAS
Labeler DUNS
634855407
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-18
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e9aa7b03-dca0-4a23-9665-4e8d1b1aa137

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 03701089520232

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121297 000