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M/L-10

FDA UDI

Class II (US FDA UDI)

by Microline Surgical, Inc.

Identity

Trade Name
M/L-10 FDA UDI
Generic Name
Open-surgery ligation clip applier FDA UDI
Device Name
M/L-10 Multi-Fire Clip Applier, Reusable FDA UDI
Model / Reference
1002R FDA UDI
Description
M/L-10 Multi-Fire Clip Applier, Reusable FDA UDI

Identifiers

Catalog Number
1002R FDA UDI
Primary DI / UDI-DI
00811099010845 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Open-surgery ligation clip applier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

M/L-10 by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae38d776-2e57-4711-a06e-f8488d6fda0e 35 fields · synced Jun 8, 2026