AccessGUDID - DEVICE: AMSure® NON-STERILE SUCTION TUBING (10704411004219)

GUDID

Device Identifier (DI) Information

Brand Name: AMSure® NON-STERILE SUCTION TUBING
Version or Model: 1
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AS829B-01
Company Name: AMSINO INTERNATIONAL, INC.

Primary DI Number: 10704411004219
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 825673239 *Terms of Use

Device Description: AMSure® NON-STERILE SUCTION TUBING NON-STERILE SUCTION TUBING, I.D. 1/4 in. (6 mm) X 100 ft. (30.5 m), CONNECTORS EVERY 6 FT. (1.8 m)

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):	Yes
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?
16779	Suction/irrigation tubing, single-use	A length of flexible noninvasive tube, typically made of synthetic polymer material(s), intended to interface between suction and/or irrigation devices (e.g., catheters, pumps, collection bottles) during a medical/surgical procedure (not dedicated to ophthalmic use); it might additionally be intended for use during reusable device reprocessing. The tubing may be provided in rolls from which required lengths are cut, or may be provided in predetermined lengths with connectors; it does not include additional associated items such as a clamp, spike, or bag (i.e., not a tubing set). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BYY	Tube, Aspirating, Flexible, Connecting

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e9da5488-b277-45ef-87ed-56f693099b34
Public Version Date: June 08, 2021
Public Version Number: 2
DI Record Publish Date: April 17, 2020