AccessGUDID - DEVICE: BONEFIT IMPLANT SYSTEM ACCESSORIES & INSTRUMENTS (07630031724298)

GUDID

Device Identifier (DI) Information

Brand Name: BONEFIT IMPLANT SYSTEM ACCESSORIES & INSTRUMENTS
Version or Model: Screws
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 048.362V4
Company Name: Institut Straumann AG

Primary DI Number: 07630031724298
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 4
Labeler D-U-N-S® Number*: 483599259 *Terms of Use

Device Description: SCS Guide screw for 048.240/241, cannot be shortened, L 8 mm, Ti

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?
61647	Dental prosthesis/implant abutment screw	A device intended to be used short- or long-term to attach a dental implant abutment and/or prosthesis (e.g., crown, bridge) to a dental implant during dental restorative procedures. It is made of metal [e.g., titanium (Ti)] and consists of a rod-like fastener inserted through the abutment/prosthesis. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
DZE	IMPLANT, ENDOSSEOUS, ROOT-FORM

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K894844	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: 0f1b0bc5-dedf-4ae5-82f9-cfb706caa58a
Public Version Date: April 21, 2023
Public Version Number: 7
DI Record Publish Date: September 24, 2015