Identity
- Trade Name
- Ambler Surgical FDA UDI
- Generic Name
- Manual intraocular lens injector, reusable FDA UDI
- Device Name
- Ambler III cartridge injector, 5 3/4'', front loading cartridge, for use with Alcon® Type D cartridges, plunger mechanism, titanium FDA UDI
- Model / Reference
- Ambler III cartridge injector FDA UDI
- Description
- Ambler III cartridge injector, 5 3/4'', front loading cartridge, for use with Alcon® Type D cartridges, plunger mechanism, titanium FDA UDI
Identifiers
- Catalog Number
- 7284T FDA UDI
- Primary DI / UDI-DI
- 00190660089641 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Manual intraocular lens injector, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Manual intraocular lens injector, reusable
Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Ambler Surgical, LLC
Sources (1)
- FDA UDI 8cb9c83f-57d3-4d21-8591-45fb718a7a28 35 fields · synced Jun 8, 2026