AccessGUDID - DEVICE: HYGITECH (03615140000406)

GUDID

Device Identifier (DI) Information

Brand Name: HYGITECH
Version or Model: HY-07011
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HY-07011
Company Name: HYGITECH

Primary DI Number: 03615140000406
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 279456896 *Terms of Use

Device Description: Total protection of the face, eyes and forehead Elastic 3 ply mask with nose clip, EN 14683 Fully transparent panoramic visor No glass fibres, latex-free, odourless . Comfortable: flexible nose piece sheathed steel 9cm High strength visor stitched to the mask Anti-fog treatment on the inside and front of the shield Doesn't affect vision during procedure Perfect protection: 30cm wrap-around visor Lightweight: 11g Can be worn with precription glasses Packed individually keeping the visors in perfect condition

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	No
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?
11961	Face splash shield, single-use	A clear, transparent guard intended to provide full face cover, to protect (shield) the healthcare worker from blood and other body fluid splashes while performing a clinical or laboratory procedure. It is commonly known as a splash shield. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FXX	Mask, Surgical

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K173062	000

Device Exempt from Premarket Submission: No 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: 669f185a-26e1-4b54-8452-e815151d1d04
Public Version Date: December 23, 2020
Public Version Number: 1
DI Record Publish Date: December 15, 2020