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Aspire Venting Tube Kit

FDA UDI

Class II (US FDA UDI)

by Aspire Bariatrics, Inc.

Identity

Trade Name
Aspire Venting Tube Kit FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
Aspire Venting Tube Kit FDA UDI
Model / Reference
100-0047 FDA UDI
Description
Aspire Venting Tube Kit FDA UDI

Identifiers

Catalog Number
100-0047 FDA UDI
Primary DI / UDI-DI
10857808005891 FDA UDI
510(k) Number
K182248 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrostomy 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

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Gastrostomy tube

Aspire Venting Tube Kit by Aspire Bariatrics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrostomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8c1ca8c7-f278-4fd6-ae23-3178084f41f3 36 fields · synced May 31, 2026