Porges Coloplast RF3019

by Coloplast A/S

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number03600040325018 UDI-DI	Date22 Jan 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Porges Coloplast
Generic Name: Nephrostomy introduction sheath
Model / Ref / Catalog: RF3019

Primary DI / UDI-DI: 03600040325018
FDA Product Code: LJE
GMDN Term: Nephrostomy introduction sheath

Device Class: U
GUDID distribution status: In Commercial Distribution

Size: Length — 19 Centimeter
Catheter Gauge — 30 French

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Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (9)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No