AccessGUDID - DEVICE: Darby Dental Supply, LLC (00889813017302)

GUDID

Device Identifier (DI) Information

Brand Name: Darby Dental Supply, LLC
Version or Model: 9510947
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9510947
Company Name: DARBY DENTAL SUPPLY, LLC

Primary DI Number: 00889813017302
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 6
Labeler D-U-N-S® Number*: 825137818 *Terms of Use

Device Description: Plastic Thermal Obturator .08 #25

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?
47750	Warm-bonded endodontic obturation system	An assembly of devices designed to deliver preheated resin-based sealing, filling, and core materials into a root canal for direct warm bonding during an endodontic obturation procedure. It typically consists of a mains electricity (AC-powered) oven used to heat the preloaded oburators, a series of root canal sizers (verifiers) used for the selection of the appropriate obturator, and preloaded obturators; other materials may be included (e.g., self-etch sealer).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EKM	GUTTA-PERCHA

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 244b0c18-1d51-48ef-8e68-685b9e20580e
Public Version Date: June 04, 2018
Public Version Number: 1
DI Record Publish Date: May 04, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: 00889813017296 CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: Yes
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(516)688-6800 ext: 6431
Email: Robyn.livingston@darby.com

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