N.A. 38636

GUDID 04049368219170

N.A.

Geuder Aktiengesellschaft

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 04049368219170
• NIH Device Record Key: a56928d0-a8e7-4e1d-93eb-031a961482d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N.A.
• Version Model Number: 38636
• Catalog Number: 38636
• Company DUNS: 316267202
• Company Name: Geuder Aktiengesellschaft
• 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: false
• 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	04049368219170 [Primary]

FDA Product Code

• HMX: Cannula, ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-03
• Device Publish Date: 2021-02-23

On-Brand Devices [N.A.]

• 04049368053446: N.A.
• 04049368221425: N.A.
• 04049368221418: N.A.
• 04049368219170: N.A.
• 04049368216445: N.A.
• 04049368216421: N.A.
• 04049368216209: N.A.
• 04049368216087: N.A.
• 04049368214526: N.A.
• 04049368210054: N.A.
• 04049368210047: N.A.
• 04049368210030: N.A.
• 04049368209973: N.A.
• 04049368209232: N.A.
• 04049368209225: N.A.
• 04049368209218: N.A.
• 04049368208495: N.A.
• 04049368208488: N.A.
• 04049368207443: N.A.
• 04049368207047: N.A.
• 04049368206934: N.A.
• 04049368202035: N.A.
• 04049368202028: N.A.
• 04049368202011: N.A.
• 04049368202004: N.A.
• 04049368201991: N.A.
• 04049368201984: N.A.
• 04049368201663: N.A.
• 04049368201533: N.A.
• 04049368197867: N.A.
• 04049368197850: N.A.
• 04049368197805: N.A.
• 04049368197799: N.A.
• 04049368193906: N.A.
• 04049368172642: N.A.
• 04049368172635: N.A.
• 04049368172628: N.A.
• 04049368172512: N.A.
• 04049368172505: N.A.
• 04049368172499: N.A.
• 04049368172482: N.A.
• 04049368172475: N.A.
• 04049368172260: N.A.
• 04049368171423: N.A.
• 04049368171416: N.A.
• 04049368171409: N.A.
• 04049368170679: N.A.
• 04049368169697: N.A.
• 04049368169680: N.A.
• 04049368166719: N.A.