← Back to catalogue

PUGGLE™ G-Tube

FDA UDI

Class II (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
PUGGLE™ G-Tube FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, sterile FDA UDI
Device Name
PUGGLE™ G-Tube 18 Fr. 20 mL GASTROSTOMY TUBE WITH Y-PORTS FDA UDI
Model / Reference
1 FDA UDI
Description
PUGGLE™ G-Tube 18 Fr. 20 mL GASTROSTOMY TUBE WITH Y-PORTS FDA UDI

Identifiers

Catalog Number
PLG18-20 FDA UDI
Primary DI / UDI-DI
00704411007305 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Enteral feeding kit, adult/paediatric, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
Not 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

Yes

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

No

FDA UDI

A comprehensive 2-3 paragraph SEO description for the PUGGLE G-Tube medical device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 31483057-45d4-4ce3-8009-5078e514ca76 35 fields · synced Oct 6, 2026