Device
6" GROOVED DIRECTOR
Manufacturer
Bausch & Lomb Incorporated
Model: E4220 15 Catalog: E4220 15 DI: 00757770460670 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: Yes OTC: No
First Published: 2026-04-29 Current Version: 2026-05-07
Description
6" GROOVED DIRECTOR
Sterilization
Method Types - Sterilization Method: Moist Heat or Steam Sterilization
Device Sterile: No
Sterilization Prior To Use: Yes
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 83028ce7-7f85-4a6c-94a5-7f128a6edb50
Distribution Status: In Commercial Distribution
DUNS Number: 196603781
Device Count: 1
DM Exempt: No
Premarket Exempt: Yes
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: No
Expiration Date Tracked: No
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Device ID: 00757770460670
Type: Primary
Issuing Agency: GS1
GMDN
Code: 35010
Name: Lacrimal dilator, reusable
Definition:
A hand-held, manual, ophthalmic surgical instrument used for enlarging the lacrimal canal (the lacrimal duct) during an ophthalmic procedure. This is a reusable device.
FDA Product Codes
HNL
Probe, Lachrymal