Severin Lacrimal Cannula 1103-500J

by Sontec Instruments, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00192896053205 UDI-DI	Date4 Oct 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name: Severin Lacrimal Cannula
Generic Name: Ophthalmic working-channel cannula, reusable
Model / Ref / Catalog: 1103-500J

Primary DI / UDI-DI: 00192896053205
FDA Product Code: HMX
GMDN Term: Ophthalmic working-channel cannula, reusable

Device Class: Class I
Regulation Number: 886.4350
GUDID distribution status: In Commercial Distribution

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

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