AccessGUDID - DEVICE: WIEDER TONGUE DEPRESSOR (00192896043923)

GUDID

Device Identifier (DI) Information

Brand Name: WIEDER TONGUE DEPRESSOR
Version or Model: 485-592S
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 485-592S
Company Name: SONTEC INSTRUMENTS, INC.

Primary DI Number: 00192896043923
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 040729840 *Terms of Use

Device Description: WIEDER TONGUE DEPRESSOR WITH SUCTION LARGE SHAFT WIDE FLARED DEPRESSING TIP

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?
14066	Tongue depressor, surgical	A hand-held surgical instrument designed to displace and maintain the tongue in a fixed position, usually by depressing it towards the floor of the mouth. It is typically a metallic (e.g., high-grade stainless steel) device either with a straight shape, or more frequently smoothly bent at its center (e.g., to a 90? arch). The proximal end is used as a handle, while the distal end (usually serrated and may include holes) is used to depress the tongue. The device is used in oral surgery (e.g., during tonsillectomy). This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMA	DEPRESSOR, TONGUE, NON-SURGICAL

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 [?]
Dry Heat Sterilization
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: 2e7f3024-c84b-49ff-b7c6-1a1403764b81
Public Version Date: October 18, 2018
Public Version Number: 1
DI Record Publish Date: September 17, 2018