AccessGUDID - DEVICE: Cortium Universal OCT Spinal Fixation System (00810076338217)

GUDID

Device Identifier (DI) Information

Brand Name: Cortium Universal OCT Spinal Fixation System
Version or Model: UU994-95-41
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Ulrich Medical Usa, Inc.

Primary DI Number: 00810076338217
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 624083866 *Terms of Use

Device Description: In-Situ Rod Bender, Ø4.0mm, Right

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?
44795	Manual orthopaedic bender, reusable	A manually-operated surgical instrument designed to bend orthopaedic devices, typically those for implantation (e.g., orthopaedic rods, bone fixation plates), to an appropriate anatomical shape. The bending process is typically performed within the operating room (OR), inside or outside of the operative sterile field. The device may be hand held or table mounted. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HXW	Bender

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K230614	000

Device Exempt from Premarket Submission: No 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
No Device Sizes

Device Record Status

Public Device Record Key: 430d6462-c4c7-4f15-85b0-4132dc888da5
Public Version Date: June 27, 2024
Public Version Number: 1
DI Record Publish Date: June 19, 2024