AccessGUDID - DEVICE: BOLD (10381780046493)

GUDID

Device Identifier (DI) Information

Brand Name: BOLD
Version or Model: 111032ND
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 111032ND
Company Name: NEWDEAL

Primary DI Number: 10381780046493
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2027
Device Count: 1
Labeler D-U-N-S® Number*: 536935331 *Terms of Use

Device Description: The BOLD SCREW is a cannulated compression screw made of a Titanium alloy. Its design includes a long non-threaded shaft, allowing optimal compression, and a self-tapping screw tip. These features enable its use in small bone fixation and its specific design allows its use in the foot. Screws come in lengths of 10-34 mm.

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":	Yes
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?
56642	Orthopaedic bone screw, non-bioabsorbable, non-sterile	A small, non-sterile, threaded rod with a slotted head typically used for internal orthopaedic fracture fixation by being screwed into bone to hold plates or nails to bone or to provide direct interfragmentary stabilization of bone, or it may fasten soft tissue to bone; it is made of a material that cannot be chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Screws available are: cortical, cancellous, malleolar, scaphoid, partially-threaded and fully-threaded, self-tapping, and cannulated. A "lag screw" can be any of these used to obtain compression. This device must be sterilized prior to use.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
HWC	Screw, fixation, bone

FDA Premarket Submission

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

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
Special Storage Condition, Specify: Store in dry place

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 3.0mm diam. x 32mm length

Device Record Status

Public Device Record Key: 8dc137eb-6475-4d23-9e5c-bba86c47d8cc
Public Version Date: February 19, 2024
Public Version Number: 6
DI Record Publish Date: October 09, 2017