AccessGUDID - DEVICE: Caulk® Post & Core Kit (D00261I0001)

GUDID

Device Identifier (DI) Information

Brand Name: Caulk® Post & Core Kit
Version or Model: 61i000
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 61i000
Company Name: DENTSPLY INTERNATIONAL INC.

Primary DI Number: D00261I0001
Issuing Agency: HIBCC
Commercial Distribution End Date: June 05, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 083235549 *Terms of Use

Device Description: Caulk® Post & Core Kit

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:	Yes
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?
37871	Crown surgical drill bit, reusable	A shaft of metal with a hollow centre designed for overdrilling a surgical screw or screw shaft to expose it for its removal, with another instrument, when the screw head has become defective or detached. The device is commonly called a "hollow mill" or "crown drill", but may also be referred to as a "hollow reamer", and is designed as a cylindrical hollow shell with a thin wall that has saw teeth at the cutting edge. It is inserted into a surgical power tool for rotation. This device may also be used to obtain core bone biopsies. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EKP	REAMER, PULP CANAL, ENDODONTIC

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: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Keep away from sunlight. Keep dry.

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 15 Fiber Posts 2 Reamers 4 Drills 1 TCGel, 25 Tips, 1 bottle adhesive & activator 1 Mixing Well 2 syringes FluoroCore 10 Mix Tips and Endo Intraoral Tips 1 Mix Pad 30 Paper Points 50 Root Canal Tips

Device Record Status

Public Device Record Key: c162fea8-6dfa-42fe-b0a2-5d8a65df60ca
Public Version Date: June 05, 2024
Public Version Number: 4
DI Record Publish Date: September 23, 2016