Identity
- Trade Name
- Millennium FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Cibri Corneal Fcp Very Delicate deg FDA UDI
- Model / Reference
- 92-F1651T FDA UDI
- Description
- Cibri Corneal Fcp Very Delicate deg FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190776204556 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
At Avalign Technologies, Inc., we're proud to introduce the Millennium, a hand-held, manual surgical instrument designed for precise ophthalmic soft-tissue manipulation. This versatile device features conventional and reverse-action tweezers-like designs with various tip configurations, allowing for effective grasping, removal, or clamping of foreign bodies from ocular tissues. With its reusable design and ability to be sterilized prior to use, the Millennium is a trusted tool in ophthalmic procedures.
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Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- AVALIGN TECHNOLOGIES, Inc.
Sources (1)
- FDA UDI 5a578ab1-1dda-42c1-9f08-a630a68b782e 34 fields · synced Aug 4, 2026