Identity
- Trade Name
- 1-Day Flat Pack TC CP90 FDA UDI
- Generic Name
- Soft corrective contact lens, daily-disposable FDA UDI
- Model / Reference
- -6.75/-0.75/180 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884465580525 FDA UDI
- FDA Product Code
- LPL FDA UDI
- GMDN Term
- Soft corrective contact lens, daily-disposable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5925 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
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Soft corrective contact lens, daily-disposable
A comprehensive medical device for correcting refractive vision conditions with a soft corrective contact lens designed to be worn directly against the cornea and adjacent limbal and scleral areas of the eye.
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Also classified as Soft corrective contact lens, daily-disposable.
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- ZonedIn Contact Lenses — ZONEDIN VISION LLC · Class II
- ZonedIn Vision Contact Lenses — ZONEDIN VISION LLC · Class II
- ZonedIn Contact Lenses — ZONEDIN VISION LLC · Class II
- ZonedIn Vision Contact Lenses — ZONEDIN VISION LLC · Class II
- ZonedIn Contact Lenses — ZONEDIN VISION LLC · Class II
- ZonedIn Vision Contact Lenses — ZONEDIN VISION LLC · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Menicon Co., Ltd.
Sources (1)
- FDA UDI 6f67b7a9-0691-4625-b5d5-b427333c1e23 32 fields · synced Jul 14, 2026