AccessGUDID - DEVICE: AMD-RITMED (10686864053290)

GUDID

Device Identifier (DI) Information

Brand Name: AMD-RITMED
Version or Model: BGTS35X23
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: BGTS35X23
Company Name: AMD Medicom Inc

Primary DI Number: 10686864053290
Issuing Agency: GS1
Commercial Distribution End Date: June 06, 2023
Device Count: 50
Labeler D-U-N-S® Number*: 256880576 *Terms of Use

Device Description: AMD-RITMED BURN DRESSING 35 1/2 X 23 Inch

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):	Yes
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?
48134	Woven gauze pad, non-antimicrobial	A non-medicated device in the form of a patch or swab (also referred to as a sponge) made from woven material (e.g., cotton, cellulose) and primarily designed to absorb fluids for medical purposes; it does not include petrolatum. It is typically used to: clean, cover, or pack wounds or abrasions and absorb their exudates; absorb body-surface exudates; or apply topical medications. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NAC	Dressing, wound, hydrophilic

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: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Cool dry place

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 35 1/2 X 23 Inch

Device Record Status

Public Device Record Key: 51a9bd39-6b03-4adc-8753-a1e76ecb6e9b
Public Version Date: April 18, 2025
Public Version Number: 3
DI Record Publish Date: January 16, 2019