DEVICE: Mini ONE® Balloon Button (00842071120696)
Device Identifier (DI) Information
Mini ONE® Balloon Button
M1-5-1023-I
In Commercial Distribution
M1-5-1023-I
APPLIED MEDICAL TECHNOLOGY, INC.
M1-5-1023-I
In Commercial Distribution
M1-5-1023-I
APPLIED MEDICAL TECHNOLOGY, INC.
10FR x 2.3 cm Mini ONE® Balloon Button (Boxed Kit -I)
Low Profile Feeding Device
Device Characteristics
| MR Conditional | |
| No | |
| Yes | |
| Yes | |
| Yes | |
| No | |
| Yes | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 38565 | Gastrostomy button |
A sterile, short, hollow tube that is inserted into the stomach percutaneously to permit long-term enteral feeding. The tube does not permit reflux and its external end is flush with abdominal skin. This is a single-use device.
|
Active | true |
| 64461 | Enteral feeding noninvasive-component set |
A collection of devices such as tubing, connectors, chambers, clamps, and bags/bottles intended to be used to create the noninvasive (i.e., fully external) portion of an enteral feeding device assembly; it is not intended for intravenous (IV) administration. 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 [?] |
|---|---|
| K945618 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| No storage/handling found |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Length: 2.3 Centimeter |
| Catheter Gauge: 10 French |
Device Record Status
74cb48dc-ddc2-4ec6-a864-be9562b1a152
July 20, 2023
2
October 11, 2019
July 20, 2023
2
October 11, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
(440)717-4000
cs@appliedmedical.net
cs@appliedmedical.net