Identity
- Trade Name
- ENSIZOR FDA UDI
- Generic Name
- Flexible endoscopic scissors, single-use FDA UDI
- Device Name
- Flexible endoscopic scissors FDA UDI
- Model / Reference
- ES26165 FDA UDI
- Description
- Flexible endoscopic scissors FDA UDI
Identifiers
- Catalog Number
- ES26165-1 FDA UDI
- Primary DI / UDI-DI
- 00860001219845 FDA UDI
- FDA Product Code
- OCZ FDA UDI
- GMDN Term
- Flexible endoscopic scissors, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 165 Centimeter FDA UDIOuter Diameter — 2.6 Millimeter FDA UDI
Category: Flexible endoscopic scissors, single-use
Ensizor by Slater Endoscopy, LLC — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Slater Endoscopy, LLC
Sources (1)
- FDA UDI 78b2d8a6-897b-4fc8-a6be-bc86b01b699b 35 fields · synced Jun 1, 2026