AccessGUDID - DEVICE: 676 - 4/Eye Pads & 4/Tape

GUDID

Device Identifier (DI) Information

Brand Name: 676 - 4/Eye Pads & 4/Tape - 8/Unit
Version or Model: R214-008
Commercial Distribution Status: In Commercial Distribution
Catalog Number: R214-008
Company Name: Certified Safety Manufacturing, Inc.

Primary DI Number: 00766588140087
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 788460483 *Terms of Use

Device Description: 676 - 4/Eye Pads & 4/Tape - 8/Unit

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:	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?
11661	Eye pad	A cushion-like device made of various materials (e.g., gauze, cotton) intended to protect the eye or to absorb eye secretions. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HMP	PAD, EYE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K940333	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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: fc73280d-7655-4826-9ebe-1a07e7663254
Public Version Date: February 06, 2023
Public Version Number: 1
DI Record Publish Date: January 27, 2023