OftalOnePack

GUDID 00850074437123

OFTAL-ONE INC.

General surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00850074437123
• NIH Device Record Key: d97306ca-7e8c-4f31-8e3a-3a0445c59fd4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OftalOnePack
• Version Model Number: PAPR 001N
• Company DUNS: 118668232
• Company Name: OFTAL-ONE INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850074437123 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

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: 2026-01-13
• Device Publish Date: 2026-01-05

Devices Manufactured by OFTAL-ONE INC.

• 00850074437048 - OftalOnePack, Oftal-One: 2026-03-06 Whole globe recovery pack for Eye Bank
• 00850074437109 - OftalOnePack, Oftal-One: 2026-03-06 Tissue processing pack for Eye Bank
• 00850074437116 - OftalOnePack, Oftal-One: 2026-03-06 Cornea recovery pack for Eye Bank
• 00850074437123 - OftalOnePack: 2026-01-13
• 00850074437123 - OftalOnePack: 2026-01-13
• 00850074437017 - Oftal-One Pack: 2025-06-17
• 00850074437000 - OftalOnePack, Oftal-One: 2025-05-26