Rpc

FDA UDI

Class I (US FDA UDI)

by Reprocessing Products Corp

Identity

Trade Name: RPC FDA UDI
Generic Name: Luer-formatted disinfection cap FDA UDI
Device Name: Injectable Catheter Cap FDA UDI
Model / Reference: 7001-3926 FDA UDI
Description: Injectable Catheter Cap FDA UDI

Identifiers

Catalog Number: 7001-3926 FDA UDI
Primary DI / UDI-DI: 00858293006014 FDA UDI
510(k) Number: K855039 FDA UDI
FDA Product Code: GCE FDA UDI
GMDN Term: Luer-formatted disinfection cap FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Luer-formatted disinfection cap

Rpc by Reprocessing Products Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K855039 also covers:

175IBLSSC — ELCAM MEDICAL ITALY SPA

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Reprocessing Products Corp

Sources (1)

FDA UDI b2216e32-857a-4699-9d23-9a9d6a84e859 35 fields · synced May 31, 2026