AccessGUDID - DEVICE: Meijer (00708820630369)

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
43090	Basic electric toothbrush	An electrically-powered device designed to be used by a patient to brush clean their teeth and gums (i.e., remove plaque, tartar, stains). It typically consists of a proximal handle and an exchangeable distal head with rows of bristles (e.g., nylon) grouped in separate tufts or evenly distributed. The device provides automated bristle movement (e.g., rotary or vibratory) intended to augment brushing, and is typically used with toothpaste. This is a reusable device.	Active	false
11158	Dental floss	A string-like device formed as thread or tape, used for the removal of plaque and/or debris from the proximal surfaces of teeth and the gingival surfaces of fixed prostheses. It is typically made of a synthetic fibre. After application, this device cannot be reused.	Active	false
33208	Periodontal pick/brush, reusable	A manual, pointed, oral hygiene device with a soft tip or bristles intended to be used to stimulate and massage the gums to promote good periodontal (gum) condition, and to clean and remove plaque and debris from between the teeth and gingival surfaces. It may also be referred to as an interdental/interproximal brush and is intended for use in the home. This is a reusable device.	Active	false

Product Code	Product Code Name
JEQ	Toothbrush, Powered
JES	Floss, Dental
JET	Pick, Massaging

Product Code

Product Code Name

JEQ

Toothbrush, Powered

JES

Floss, Dental

JET

Pick, Massaging

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

FDA Premarket Submission Number [?]

Supplement Number [?]

Premarket Submission Number Not Available/Not Released

Sterilization Method [?]
No Sterilization Methods Found

Sterilization Method [?]

No Sterilization Methods Found

Storage and Handling
No storage/handling found

Storage and Handling

No storage/handling found

Size Type Text
No Device Sizes

Size Type Text

No Device Sizes

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
40708820630367	4	00708820630369		In Commercial Distribution	inner
20708820630363	6	40708820630367		In Commercial Distribution	shipper

Package DI Number

Quantity per Package

Contains DI Package

Package Discontinue Date

Package Status

Package Type

40708820630367

00708820630369

In Commercial Distribution

inner

20708820630363

40708820630367

In Commercial Distribution

shipper

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

Issuing Agency [?]

Secondary DI Number

No Secondary DIs found

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):	No
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

DEVICE: Meijer (00708820630369)

Device Identifier (DI) Information

Device Characteristics

GMDN

FDA Product Code

FDA Premarket Submission

Sterilization

Storage and Handling

Clinically Relevant Size

Device Record Status

Alternative and Additional Identifiers Additional Identifiers

Package DI

Secondary DI

Unit of Use DI

Direct Marking (DM)

Production Identifier(s) in UDI

Customer Contact