AccessGUDID - DEVICE: Parkell® (10810000527530)

GUDID

Device Identifier (DI) Information

Brand Name: Parkell®
Version or Model: S150L
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: S150L
Company Name: PARKELL, INC.

Primary DI Number: 10810000527530
Issuing Agency: GS1
Commercial Distribution End Date: June 24, 2021
Device Count: 3
Labeler D-U-N-S® Number*: 009900424 *Terms of Use

Device Description: Large Posterior Dry Field Mouth Props (Set of 3 Props)

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:	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?
44827	Dental dry field kit	A collection of devices and supplies used in orthodontic and restorative dentistry to maintain a dry oral cavity for treatment procedures. It provides the operator with easy access to the field of operation by holding the mouth open, displacing the tongue, and removing saliva during various procedures (e.g., bonding orthodontic brackets, bleaching, applying veneers or pit and fissure sealants, posterior restorations). It typically consists of bite blocks, pad extenders, suction tips of varying sizes, and tubing that connects to a suction system. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EIG	Retractor, All Types

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: 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: 24890213-7adb-4df6-9889-69f84d4d3a68
Public Version Date: August 26, 2021
Public Version Number: 2
DI Record Publish Date: April 05, 2019

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: 00810000527533 CLOSE

Direct Marking (DM)

[?]

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

Production Identifier(s) in UDI

[?]

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

Customer Contact

[?]

Phone: 631-249-1134
Email: customerservice@parkell.com

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