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Fenestrated Bowel Grasper, 35cm, 20mm Jaw

FDA UDI

Class II (US FDA UDI)

by Encision, Inc.

Identity

Trade Name
Fenestrated Bowel Grasper, 35cm, 20mm Jaw FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
Fenestrated Bowel Grasper, 35cm, 20mm Jaw FDA UDI
Model / Reference
EP3690RR FDA UDI
Description
Fenestrated Bowel Grasper, 35cm, 20mm Jaw FDA UDI

Identifiers

Catalog Number
EP3690RR FDA UDI
Primary DI / UDI-DI
10815288013812 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic electrosurgical electrode, monopolar, reusable

Fenestrated Bowel Grasper, 35cm, 20mm Jaw by Encision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Encision, Inc.

Sources (1)

  • FDA UDI 3cdf18df-aacc-4eab-9963-5fa798cb3153 34 fields · synced May 30, 2026