FDA UDI Not in Commercial Distribution 🇺🇸 United States

Titan™

DI: 10381780489160 · Model: TITANREVSPBIMP · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titan™
Primary DI
10381780489160
Version / Model
TITANREVSPBIMP
Catalog Number
TITANREVSPBIMP
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-05
Public Version
2
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
ef8d80fa-52a2-4c0e-a2fd-91fea518ea95
Distribution End Date
2023-03-31

Device Description

TITAN Reverse Shoulder System Instruments

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary 10381780489160

Customer Contacts