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AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Indivi

FDA UDI

Class II (US FDA UDI)

by Andersen Products, Inc.

Identity

Trade Name
AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Indivi FDA UDI
Generic Name
Nasogastric/orogastric tube FDA UDI
Device Name
AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Individual) FDA UDI
Model / Reference
AN22.00 FDA UDI
Description
AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Individual) FDA UDI

Identifiers

Primary DI / UDI-DI
05060171440352 FDA UDI
510(k) Number
K011077 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric/orogastric tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasogastric/orogastric tube

AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Indivi by Andersen Products, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Nasogastric/orogastric tube.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf542eee-29cd-4110-a6a6-54615c2d758f 34 fields · synced May 30, 2026