AccessGUDID - DEVICE: CAPTURE™ (10381780242123)

GUDID

Device Identifier (DI) Information

Brand Name: CAPTURE™
Version or Model: AW-3005
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AW3005
Company Name: Ascension Orthopedics, Inc.

Primary DI Number: 10381780242123
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: CAPTURE™ High Torque Screw System The cannula cleaning stylet is used to clean all cannulated instruments. This instrument is used with 7.0 mm instruments.

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:	Yes
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?
35589	Intramedullary canal cleaning brush, reusable	A hand-held manual surgical instrument designed to remove blood clots and bone debris from the intramedullary canal of a bone (marrow space) in preparation for the insertion of orthopaedic cement. It typically consists of a handle at the proximal end and bristles, fibres, or spines at the distal end which may be soft or stiff and are mounted along a single plane or radiate out around a central shaft which may be flexible or rigid. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

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: 3.2 mm dia

Device Record Status

Public Device Record Key: ab7d7acf-377f-4c28-9f7d-b58beb4caa42
Public Version Date: February 22, 2023
Public Version Number: 4
DI Record Publish Date: August 30, 2017