Lidstick

GUDID 04049584032454

OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung

Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator Meibomian gland manual expressor/evaluator

• Primary Device ID: 04049584032454
• NIH Device Record Key: cd325796-85e4-4dc0-8e5b-02130cc5a162
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lidstick
• Version Model Number: 77500
• Company DUNS: 317138956
• Company Name: OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049584032454 [Primary]
GS1	04049584032959 [Package]; Package: Individual roll [100 Units]; In Commercial Distribution
GS1	04049584032966 [Package]; Contains: 04049584032959; Package: Box [2 Units]; In Commercial Distribution
GS1	04049584032973 [Package]; Contains: 04049584032966; Package: Shipper [16 Units]; In Commercial Distribution

FDA Product Code

• HNI: Retractor, Ophthalmic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-26
• Device Publish Date: 2023-06-16

Devices Manufactured by OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung

• 04049584005878 - Lorgnette with striated lenses (Bagolini), Axes 45°/123°: 2023-06-26
• 04049584032454 - Lidstick: 2023-06-26
• 04049584032454 - Lidstick: 2023-06-26
• 04049584033048 - GONIO ready® 200 for f=200: 2023-04-04 GONIO ready® 200 for f=200
• 04049584034489 - GONIO ready® 175 for f=175: 2023-04-04 GONIO ready® 175 for f=175
• 04049584001030 - BK X/O (according to Kochniss), without convex cylinders, coated, inclusive tria: 2022-12-15 BK X/O (according to Kochniss), without convex cylinders, coated, inclusive trial lens case
• 04049584001078 - Prism Lens Case, coated: 2022-12-15 Prism Lens Case, coated
• 04049584001153 - Prism Lens Case S, coated: 2022-12-15 Prism Lens Case S, coated
• 04049584001191 - BK 1/T, table version, trial lens case: 2022-12-15 BK 1/T, table version, trial lens case