← Back to catalogue

Aspire Introducer Needle

FDA UDI

Class II (US FDA UDI)

by Aspire Bariatrics, Inc.

Identity

Trade Name
Aspire Introducer Needle FDA UDI
Generic Name
Non-vascular catheter introduction set FDA UDI
Device Name
Introducer Needle FDA UDI
Model / Reference
100-0035 FDA UDI
Description
Introducer Needle FDA UDI

Identifiers

Catalog Number
100-0035 FDA UDI
Primary DI / UDI-DI
10857808005419 FDA UDI
510(k) Number
K180725 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Non-vascular catheter introduction set 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

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

Dimensions & Sizes

Size
Length — 10 Centimeter FDA UDI
Needle Gauge — 17 Gauge FDA UDI

Category: Non-vascular catheter introduction set

Aspire Introducer Needle by Aspire Bariatrics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-vascular catheter introduction set.

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 dc9b683f-dd5a-4429-b8fd-4dea8a4ee933 36 fields · synced May 30, 2026