Na 81102

by Medtronic PS Medical

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

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	Number00673978230436 UDI-DI	Date24 Nov 2015Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Lumbar cerebrospinal fluid drainage catheterization kit
Model / Reference: 81102

Primary DI / UDI-DI: 00673978230436
510(k) Number: K911382
FDA Product Code: MAJ
GMDN Term: Lumbar cerebrospinal fluid drainage catheterization kit

Device Class: Class II
Regulation Number: 868.5120
GUDID distribution status: In Commercial Distribution

Size: Length — 80.0 Centimeter

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Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number

Other properties (10)

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