Identity
- Trade Name
- Centurion FDA UDI
- Generic Name
- Eye dropper, single-use FDA UDI
- Device Name
- EYE DROPPER KIT FDA UDI
- Model / Reference
- D100ST FDA UDI
- Description
- EYE DROPPER KIT FDA UDI
Identifiers
- Catalog Number
- D100ST FDA UDI
- Primary DI / UDI-DI
- 00653160010671 FDA UDI
- FDA Product Code
- KYW FDA UDI
- GMDN Term
- Eye dropper, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6430 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
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
Category: Eye dropper, single-use
Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye dropper, single-use.
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Eye-Cept Rewetting Drops — Optics Laboratory, Inc. · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Centurion Medical Products
Sources (1)
- FDA UDI 241f6c3a-a592-4810-abb8-625a41f3958c 35 fields · synced Jun 1, 2026