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ReNew

FDA UDI

Class II (US FDA UDI)

by Microline Surgical, Inc.

Identity

Trade Name
ReNew FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Cobra Tooth Grasper Tip, Reusable FDA UDI
Model / Reference
3411 FDA UDI
Description
Cobra Tooth Grasper Tip, Reusable FDA UDI

Identifiers

Catalog Number
3411 FDA UDI
Primary DI / UDI-DI
00811099011828 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, 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: Rigid endoscopic tissue manipulation forceps, reusable

ReNew by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microline Surgical, Inc.

Sources (1)

  • FDA UDI f3a603de-f9d3-41fc-8c5a-942b28a42fc1 34 fields · synced May 31, 2026