AccessGUDID - DEVICE: FASSIER-DUVAL TELESCOPIC IM SYSTEM (07540194007155)

GUDID

Device Identifier (DI) Information

Brand Name: FASSIER-DUVAL TELESCOPIC IM SYSTEM
Version or Model: PRO164
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PRO164
Company Name: Orthopediatrics Canada ULC

Primary DI Number: 07540194007155
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 243298854 *Terms of Use

Device Description: PROBE Ø6.4mm

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?
47901	Bone nail trial, reusable	A copy of a final orthopaedic bone nail designed to be introduced into the bone (e.g., proximal and/or distal end of the intramedullary canal of a long bone) to function as a reference for the subsequent introduction of the final bone nail, and typically also guide wire and/or bone screws. It is typically used in conjunction with appropriate holders/positioning devices (not included). This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HTJ	GAUGE, DEPTH

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
Special Storage Condition, Specify: keep at room temperature

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 95c3a169-c978-42a2-ac8d-b80928a86a32
Public Version Date: May 13, 2025
Public Version Number: 8
DI Record Publish Date: May 06, 2020