← Back to catalogue

Fast1

FDA UDI

Class II (US FDA UDI)

by Pyng Medical Corp.

Identity

Trade Name
FAST1 FDA UDI
Generic Name
Intraosseous infusion kit FDA UDI
Device Name
Intraosseous Infusion System FDA UDI
Model / Reference
FAST1 Unit FDA UDI
Description
Intraosseous Infusion System FDA UDI

Identifiers

Primary DI / UDI-DI
10878353000018 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Intraosseous infusion kit 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: Intraosseous infusion kit

Fast1 by Pyng Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraosseous infusion kit.

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

Manufacturer
Pyng Medical Corp.

Sources (1)

  • FDA UDI d00e45b1-038b-49dd-93a1-6fc5c3f4c952 33 fields · synced May 30, 2026