AccessGUDID - DEVICE: AN11 - Andersen Nasogastric Tube, Pediatric, 10 Fr. (Overpack 250 Ct.) (05060171440468)

GUDID

Device Identifier (DI) Information

Brand Name: AN11 - Andersen Nasogastric Tube, Pediatric, 10 Fr. (Overpack 250 Ct.)
Version or Model: AN11.00
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: ANDERSEN PRODUCTS, INC.

Primary DI Number: 05060171440468
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 041867342 *Terms of Use

Device Description: AN11 - Andersen Nasogastric Tube, Pediatric, 10 Fr. (Overpack 250 Ct.)

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):	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?
38561	Nasogastric/orogastric tube	A sterile, hollow cylinder that can be introduced into the gastrointestinal (GI) tract both nasally and orally for feeding and/or aspiration. It is made of plastic or rubber and is available in a variety of designs and lengths. Some types are a simple rubber tube with a glass window; other types can be radiopaque to assist accurate placement, have multiple flow-through eyes, and dual connectors (e.g., one for suction and the other for irrigation/feeding). Other uses can be to decompress the stomach, withdraw specimens for diagnostic analysis, administer medications, and for irrigation of the stomach to treat upper gastrointestinal (UGI) bleeding. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNT	Tubes, Gastrointestinal (And Accessories)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K021493	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: 48f1acab-c75d-4610-b43b-4113302c1e1f
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: January 24, 2017