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Micasept Clip Applicator

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICASEPT CLIP APPLICATOR FDA UDI
Generic Name
Open-surgery ligation clip applier FDA UDI
Device Name
MICASEPT CLIP APPLICATOR FOR TITANIUM CLIPS SMALL FDA UDI
Model / Reference
26932-10 FDA UDI
Description
MICASEPT CLIP APPLICATOR FOR TITANIUM CLIPS SMALL FDA UDI

Identifiers

Catalog Number
26932-10 FDA UDI
Primary DI / UDI-DI
00192896008977 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery ligation clip applier 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 360 Millimeter FDA UDI

Category: Open-surgery ligation clip applier

Micasept Clip Applicator by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery ligation clip applier.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8badb4d5-1c1c-4fba-9f0b-2664cc0f4025 37 fields · synced Jun 1, 2026