Subcutaneous Guidewire - Large 41.240.503

by Arkis Biosciences Inc.

Listed FDA GUDID listing, not in commercial distribution

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	Number10866614000198 UDI-DI	Date14 Dec 2018Listed	StatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Subcutaneous Guidewire - Large
Generic Name: Subcutaneous tunneller, single-use
Model / Ref / Catalog: 41.240.503

Primary DI / UDI-DI: 10866614000198
FDA Product Code: GYK, MDM, HAO
GMDN Term: Subcutaneous tunneller, single-use

Device Class: Class I
Regulation Number: 882.4545, 878.4800, 882.4535
GUDID distribution status: Not in Commercial Distribution

MRI Safety: MR Unsafe

Other devices from Arkis Biosciences Inc.

SureFlo EVD Catheter Open recall

Class II

Properties

Sterile
Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (8)

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