Identity
- Trade Name
- Disposable Instruments FDA UDI
- Generic Name
- Lens loop, single-use FDA UDI
- Device Name
- Irrigating Vectis, 24g x 5.5mm Wide, 3 Ports FDA UDI
- Model / Reference
- 4029A FDA UDI
- Description
- Irrigating Vectis, 24g x 5.5mm Wide, 3 Ports FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845819004883 FDA UDI
- FDA Product Code
- HMX FDA UDI
- GMDN Term
- Lens loop, single-use 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
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Category: Lens loop, single-use
A comprehensive medical device directory listing for the Disposable Instruments, a single-use hand-held instrument designed for eye lens extraction and gentle manipulation and/or irrigation of eye tissues during an ophthalmic surgical procedure.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
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
- OASIS Medical, Inc.
Sources (1)
- FDA UDI 2e166ca3-d560-4dbd-b0e7-e6d2a3e434e1 34 fields · synced Jul 10, 2026