Traumatic Grasper, 35cm EP3020RR

by Encision, Inc.

Traumatic Grasper, 35cm EP3020RR is a Class II device made by Encision, Inc., listed in FDA GUDID since 8 Feb 2018 (UDI-DI 10815288013829), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10815288013829 UDI-DI	Date8 Feb 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10815288013829

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Traumatic Grasper, 35cm
Generic name: Endoscopic electrosurgical electrode, monopolar, reusable
Model / Ref / Catalog: EP3020RR

Primary DI / UDI-DI: 10815288013829
FDA product code: GEI
GMDN term: Endoscopic electrosurgical electrode, monopolar, reusable

Device class: Class II
Regulation number: 878.4400
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number
Manufacturing date

Other properties (11, all answered No)