AccessGUDID - DEVICE: STRAUMANN MAGELLAN(TM) ABUTMENT,PROTECTIVE CAP, COPINGS, BASAL SCREW (07630031710765)

GUDID

Device Identifier (DI) Information

Brand Name: STRAUMANN MAGELLAN(TM) ABUTMENT,PROTECTIVE CAP, COPINGS, BASAL SCREW
Version or Model: Protective caps
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 024.4323-04
Company Name: Institut Straumann AG

Primary DI Number: 07630031710765
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 483599259 *Terms of Use

Device Description: Protective cap for screw-retained abutment, D 4.6mm, H 5.1mm, PEEK/TAN

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?
44880	Dental implant suprastructure, temporary, preformed, single-use	A prefabricated device intended to be used during dental implant restorative and laboratory procedures to provide a temporary intermediate fixture level between a dental implant and a temporary dental prosthesis/restoration, during the oral soft-tissue healing and sculpturing period, prior to the fabrication/rehabilitation and installation of the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It typically includes burnout/temporary cylinders, fixture impression pick-ups, replica devices, caps/cover screws in a variety of shapes, sizes, and materials [e.g., titanium (Ti), plastic]. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
NHA	ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K133421	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
Device Size Text, specify: H 5.1mm
Outer Diameter: 4.6 Millimeter

Device Record Status

Public Device Record Key: 6ee59e7e-2af3-4863-9522-14ebf7f8801e
Public Version Date: April 04, 2019
Public Version Number: 5
DI Record Publish Date: September 24, 2015