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Microline

FDA UDI

Class II (US FDA UDI)

by Microline Surgical, Inc.

Identity

Trade Name
Microline FDA UDI
Generic Name
Electrosurgical handpiece, single-use FDA UDI
Device Name
5mm STLS Thermal Ligating Shears FDA UDI
Model / Reference
102-138D FDA UDI
Description
5mm STLS Thermal Ligating Shears FDA UDI

Identifiers

Catalog Number
102-138D FDA UDI
Primary DI / UDI-DI
00811099011415 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Microline 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 5eb39324-b1c2-4794-a640-37941f5f02fe 35 fields · synced May 30, 2026