AccessGUDID - DEVICE: AMD-RITMED ALL GAUZE (10686864041471)

GUDID

Device Identifier (DI) Information

Brand Name: AMD-RITMED ALL GAUZE
Version or Model: 6009-DX
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 6009-DX
Company Name: AMD Medicom Inc

Primary DI Number: 10686864041471
Issuing Agency: GS1
Commercial Distribution End Date: September 28, 2023
Device Count: 200
Labeler D-U-N-S® Number*: 256880576 *Terms of Use

Device Description: AMD-RITMED ALL GAUZE SPONGE12 PLY X-RAY DETECTABLE 8 X 4 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?
38496	Radiopaque woven surgical sponge	A non-medicated device made from woven gauze (e.g., cotton, cellulose) primarily intended to be used inside the body, on a surgical incision or applied to internal organs or structures to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination during a procedure; also referred to as a laparotomy sponge, it may also be used for prepping the patient. It contains an x-ray detectable marker [e.g., a thread or strand(s)] to help detect gossypiboma (sponge left inside patient). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GDY	GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

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: 8 X 4 Inch

Device Record Status

Public Device Record Key: afd830d6-ae54-4b56-a857-b2e91bf54f4f
Public Version Date: September 29, 2023
Public Version Number: 2
DI Record Publish Date: January 14, 2019