AccessGUDID - DEVICE: HYGITECH (03615140000161)

GUDID

Device Identifier (DI) Information

Brand Name: HYGITECH
Version or Model: HY-07003
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HY-07003
Company Name: HYGITECH

Primary DI Number: 03615140000161
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 279456896 *Terms of Use

Device Description: Complete article: Autoclavable frame, single use shields Anti-fog treatment Vertical inclination Frame available in 3 colours: white, blue, pink Light: 22 grams Comfortable frame, it adapts to all face types Handy: Shields easy to fit Perfect protection: 30cm shield protects the whole face The shield assures clear vision, Abrasion and scratch-resistant

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: 58b4e826-5ff5-418e-a55a-5e28309145d9
Public Version Date: December 22, 2020
Public Version Number: 1
DI Record Publish Date: December 14, 2020