AccessGUDID - DEVICE: NETCELL (05060165013166)

GUDID

Device Identifier (DI) Information

Brand Name: NETCELL
Version or Model: 37-416
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: NETWORK MEDICAL PRODUCTS LIMITED

Primary DI Number: 05060165013166
Issuing Agency: GS1
Commercial Distribution End Date: April 16, 2025
Device Count: 250
Labeler D-U-N-S® Number*: 458670304 *Terms of Use

Device Description: NETCELL Cellulose Points 10's

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?
13704	Ophthalmic sponge	A device made of absorbent material, e.g., gauze, cotton or cellulose, intended to be used to absorb excess fluid produced by the eye during microsurgical procedures and ophthalmic surgery such as cataract surgery and laser assisted in situ keratomileusis (LASIK) procedures. Some types can be used as an eyelid and lash guard and are typically shaped for use in conjunction with an eye speculum. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HOZ	Sponge, Ophthalmic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K130117	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: 57939b60-4c2d-41ad-9783-1c9707fc29c4
Public Version Date: April 17, 2025
Public Version Number: 4
DI Record Publish Date: August 28, 2019