FDA.reportPublic FDA data

ReNew XR Handpiece with Reference Length Markings

Primary DI
00811099014263
Brand
ReNew XR Handpiece with Reference Length Markings
Company
MICROLINE SURGICAL, INC.
Model
3941M
Published
2024-05-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K234147000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K234147000ReNew XR Handpiece, 25cm, with Reference Markings (3943M); ReNew XR Handpiece, 34cm, with Reference Markings (3941M); ReNew XR Handpiece, 42cm, with Reference Markings (3942M); ReNew XR Handpiece, Ratcheted, 25cm, with Reference Markings (3946M); ReNew XR Handpiece, Ratcheted, 34cm, with Reference Markings (3944M); ReNew XR Handpiece, Ratcheted, 42cm, with Reference Markings (3945M)Microline Surgical, Inc.2024-04-23GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00811099014263PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00811099014263008110990142638110990142630811099014263

GMDN Terms#

Term, Definition table
TermDefinition
Electrosurgical handpiece, reusableA hand-held component of an electrosurgical system intended to provide an electrical connection between the system generator and a detachable electrode at its distal end, enabling the surgeon controlled manipulation of the electrode during surgery; the electrode is not included. The device is typically in the form of a pen with permanently attached cables for connection to the generator; it is not intended for use during inert gas-enhanced electrosurgery. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
184080570
Device count
1
Serial number
true
Manufacturing date on label
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00811099014386REVEEL - Endoscopic Retractor - PercutaneousRV0930012025-09-22
00811099014416REVEEL - Endoscopic Retractor - TrocarRT0830012025-09-22
00811099014393REVEEL - Endoscopic Retractor - PercutaneousRV0930012025-09-22
00811099014423REVEEL - Endoscopic Retractor - TrocarRT0830012025-09-22
00811099014348ReNew Disposable Tenaculum Tip (5mm)33922025-09-09
00811099014362ReNew Disposable Tenaculum Tip (10mm)34222025-09-09
00811099014331ReNew Disposable Tenaculum Tip (5mm)33922025-09-09
00811099014355ReNew Disposable Tenaculum Tip (10mm)34222025-09-09
00811099014294ReNew XR Handpiece with Reference Length Markings3944M2024-05-03
00081109901429ReNew XR Handpiece with Reference Length Markings3944M2024-05-03
00811099014256ReNew XR Handpiece with Reference Length Markings3943M2024-05-03
00811099014270ReNew XR Handpiece with Reference Length Markings3942M2024-05-03
00811099014287ReNew XR Handpiece with Reference Length Markings3946M2024-05-03
00811099014300ReNew XR Handpiece with Reference Length Markings3945M2024-05-03
00811099013822ReNew XR353035302023-06-07
00811099013839ReNew XR353135312023-06-07
00811099013846ReNew XR35322023-06-07
00811099013853ReNew XR35332023-06-07
00811099011408Microline102-137D102-137D2017-11-13
00811099011415Microline102-138D102-138D2017-11-13

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