Identity
- Trade Name
- Ambler Surgical FDA UDI
- Generic Name
- Open-surgery dissector FDA UDI
- Device Name
- Ambler LASIK bow dissector, 4 1/2'', straight, 10.0mm wide, round handle, titanium FDA UDI
- Model / Reference
- Ambler LASIK bow dissector FDA UDI
- Description
- Ambler LASIK bow dissector, 4 1/2'', straight, 10.0mm wide, round handle, titanium FDA UDI
Identifiers
- Catalog Number
- 6097T FDA UDI
- Primary DI / UDI-DI
- 00190660106591 FDA UDI
- FDA Product Code
- GDI FDA UDI
- GMDN Term
- Open-surgery dissector 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: Open-surgery dissector
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 d26b32a1-c4a6-49a6-b009-2471c9a76fae 35 fields · synced May 30, 2026