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Infusion Safety Products, Inc.

FDA UDI

Class II (US FDA UDI)

by Infusion Safety Products, Inc.

Identity

Trade Name
Infusion Safety Products, Inc. FDA UDI
Generic Name
Vascular port administration set FDA UDI
Device Name
19ga x 1.50" RA, Non-Coring Safety Huber Needle Infusion Set with 7.5" tubing, Latex Free, Non-DEHP Tubing, Lipid Resistant, Rated to 300 psi, Approx. Priming Volume .25cc FDA UDI
Model / Reference
ISP1915 FDA UDI
Description
19ga x 1.50" RA, Non-Coring Safety Huber Needle Infusion Set with 7.5" tubing, Latex Free, Non-DEHP Tubing, Lipid Resistant, Rated to 300 psi, Approx. Priming Volume .25cc FDA UDI

Identifiers

Primary DI / UDI-DI
00856673008030 FDA UDI
510(k) Number
K170881 FDA UDI
FDA Product Code
PTI FDA UDI
GMDN Term
Vascular port administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Category: Vascular port administration set

Infusion Safety Products, Inc. by Infusion Safety Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular port administration set.

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 726b1993-9b4f-4b7e-b90b-8c33e72922a1 35 fields · synced May 30, 2026