FDA UDI In Commercial Distribution 🇺🇸 United States

Titan™

DI: 10381780245476 · Model: HDL096006701 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Titan™
Primary DI
10381780245476
Version / Model
HDL096006701
Catalog Number
HDL-0960-067-01
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-30
Public Version
6
Public Version Date
2023-02-22
Public Version Status
Update
Public Device Record Key
58c9a022-0e9a-4753-ac52-3f089740ceb8
Distribution End Date
2026-12-31

Device Description

Titan™ Reverse Shoulder System The handle is used to remove glenospheres.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Secondary M269HDL0960067011
Primary 10381780245476

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10.4 in x .255in diameter