AccessGUDID - DEVICE: Titan™ (10381780246688)

GUDID

Device Identifier (DI) Information

Brand Name: Titan™
Version or Model: PRS-0923-073-002
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PRS-0923-073-002
Company Name: Ascension Orthopedics, Inc.

Primary DI Number: 10381780246688
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2026
Device Count: 1
Labeler D-U-N-S® Number*: 942377524 *Terms of Use

Device Description: Titan™ Total Shoulder System The cement pressurizer is used to impact the cement into the prepared hole.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
46031	Orthopaedic cement compressor	A device used to apply pressure to orthopaedic bone cement during a total hip arthroplasty (THA) procedure (within the acetabulum and/or femur) in order to optimise inner bone (cancellous) cement interdigitation to improve fixation of the implant. The device is typically made of a compressible silicone rubber which conforms to the shape of the cut bone to enable formation of a good seal. Cement may be injected through the device into the bone cavity using an appropriate syringe; pressure may be applied to the device with a firm handle (e.g., stainless steel), or a backplate. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HWA	IMPACTOR

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Size M/L; 1.45 in L

Device Record Status

Public Device Record Key: 24b2ff7c-3425-4fb5-9e2c-6dbf4db55235
Public Version Date: January 25, 2023
Public Version Number: 3
DI Record Publish Date: August 30, 2017