AccessGUDID - DEVICE: Distal Jet (00190746075612)

GUDID

Device Identifier (DI) Information

Brand Name: Distal Jet
Version or Model: 855-608
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 855-608
Company Name: AMERICAN ORTHODONTICS CORPORATION

Primary DI Number: 00190746075612
Issuing Agency: GS1
Commercial Distribution End Date: June 16, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 044668515 *Terms of Use

Device Description: DISTAL JET ACTIVATION LOCK 10/PKG

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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?
64769	Orthodontic palate expander/teeth aligner, bonded	An orthodontic device intended to gradually spread the maxillary arch and/or improve teeth alignment. It is typically in the form of either: 1) a segmented body separated by a palate expander screw; or 2) a spring-like mechanism, positioned in the palate cavity with wires extending laterally, ending in bonded teeth-engaging bands. It is intended to remain in the oral cavity for the duration of treatment (fixed), and may be periodically adjusted by an orthodontist to effect skeletal and/or dental changes. This is a single-patient device intended to be used for the duration of treatment (single-use) before being discarded.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DYJ	RETAINER, SCREW EXPANSION, ORTHODONTIC

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: fa3cdcbc-672f-405d-a212-02c37ce11ac7
Public Version Date: June 16, 2025
Public Version Number: 5
DI Record Publish Date: June 24, 2019