Identity
- Trade Name
- Raptor FDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- The disposable Raptor grasping device is used to grasp tissue and/or retrieve foreign bodies, excised tissue and stents during endoscopic procedures. FDA UDI
- Model / Reference
- 00711177 FDA UDI
- Description
- The disposable Raptor grasping device is used to grasp tissue and/or retrieve foreign bodies, excised tissue and stents during endoscopic procedures. FDA UDI
Identifiers
- Catalog Number
- 00711177 FDA UDI
- Primary DI / UDI-DI
- 00816765011317 FDA UDI
- FDA Product Code
- OCZ FDA UDIPTS FDA UDI
- GMDN Term
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 230 Centimeter FDA UDIOuter Diameter — 2.4 Millimeter FDA UDI
Raptor by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI 39171b33-0f98-4cd6-ba27-2e9580fedf88 38 fields · synced May 30, 2026