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ReNew

FDA UDI

Class II (US FDA UDI)

by Microline Surgical, Inc.

Identity

Trade Name
ReNew FDA UDI
Generic Name
Ligation clip, metallic FDA UDI
Device Name
Clip/Scissor Procedure Kit, M/L-10 Cartridge 19 clips(1), Endocut Scissor Tip (1) FDA UDI
Model / Reference
1242 FDA UDI
Description
Clip/Scissor Procedure Kit, M/L-10 Cartridge 19 clips(1), Endocut Scissor Tip (1) FDA UDI

Identifiers

Catalog Number
1242 FDA UDI
Primary DI / UDI-DI
00811099010500 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Ligation clip, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ligation clip, metallic

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

Similar devices

Also classified as Ligation clip, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a24ea18b-73cb-4bee-aea0-5f582b56402c 34 fields · synced May 30, 2026