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LiV™ Instruments

FDA UDI

Class I (US FDA UDI)

by Atricure, Inc.

Identity

Trade Name
LiV™ Instruments FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
LiV Resano Grasper Strong, Standard FDA UDI
Model / Reference
001-340-7824 FDA UDI
Description
LiV Resano Grasper Strong, Standard FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00818354013276 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 25 Centimeter FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, reusable

LiV™ Instruments by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atricure, Inc.

Sources (1)

  • FDA UDI 1da0788d-695e-4a8c-98cb-c0e8acae1660 36 fields · synced Jun 1, 2026