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Procedure Products Adapters

FDA UDI

Class II (US FDA UDI)

by Procedure Products, Inc.

Identity

Trade Name
Procedure Products Adapters FDA UDI
Generic Name
Intravenous fluid bag spike FDA UDI
Device Name
I.V. UNIVERSAL STANDARD TUBING SPIKE FDA UDI
Model / Reference
47-722 FDA UDI
Description
I.V. UNIVERSAL STANDARD TUBING SPIKE FDA UDI

Identifiers

Catalog Number
47-722 FDA UDI
Primary DI / UDI-DI
B160477221 FDA UDI
510(k) Number
K910673 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Intravenous fluid bag spike FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 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: Intravenous fluid bag spike

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

Similar devices

Also classified as Intravenous fluid bag spike.

Cleared under the same submission

K910673 also covers:

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
Procedure Products, Inc.

Sources (1)

  • FDA UDI d3068392-55e5-42ce-9bf1-72323d06fb7f 35 fields · synced May 30, 2026