Personal Catheter™ Intermittent Catheter 61310

by C. R. Bard, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00801741068935 UDI-DI	Date23 Jul 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Personal Catheter™ Intermittent Catheter
Generic Name: Single-administration urethral drainage catheter
Model / Ref / Catalog: 61310

Primary DI / UDI-DI: 00801741068935
FDA Product Code: KOD
GMDN Term: Single-administration urethral drainage catheter

Device Class: Class II
Regulation Number: 876.5130
GUDID distribution status: In Commercial Distribution

Size: Catheter Gauge — 10 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