Identity
- Trade Name
- AutoDrop FDA UDI
- Generic Name
- Eye dropper bottle aid FDA UDI
- Device Name
- AutoDrop Eye Guide FDA UDI
- Model / Reference
- OP 6000 FDA UDI
- Description
- AutoDrop Eye Guide FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00384706000015 FDA UDI
- FDA Product Code
- KCM FDA UDI
- GMDN Term
- Eye dropper bottle aid FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5220 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Eye dropper bottle aid
AutoDrop by Owen Mumford Usa Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye dropper bottle aid.
- AutoSqueeze — OWEN MUMFORD USA INCORPORATED · Class I
- AutoDrop — OWEN MUMFORD USA INCORPORATED · Class I
- AutoSqueeze — OWEN MUMFORD USA INCORPORATED · Class I
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
- Owen Mumford Usa Incorporated
Sources (1)
- FDA UDI f4a6fdb1-2d05-44bd-8166-2306a006a4cb 33 fields · synced May 30, 2026