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Raptor

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

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
00724995183653 FDA UDI
FDA Product Code
PTS FDA UDI
OCZ 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
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 UDI
Outer Diameter — 2.4 Millimeter FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-use

Raptor by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI 6d54f1e1-f180-43b7-8b76-bba9667d5394 37 fields · synced Jun 8, 2026