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MICA Appliers

FDA UDI

Class I (US FDA UDI)

by Vitalitec International, Inc.

Identity

Trade Name
MICA Appliers FDA UDI
Generic Name
Open-surgery ligation clip applier FDA UDI
Device Name
REUSABLE MI CLIP APPLIER SMALL YELLOW FDA UDI
Model / Reference
PJM135-1 FDA UDI
Description
REUSABLE MI CLIP APPLIER SMALL YELLOW FDA UDI

Identifiers

Catalog Number
PJM135-1 FDA UDI
Primary DI / UDI-DI
00850001784993 FDA UDI
FDA Product Code
HBT FDA UDI
GMDN Term
Open-surgery ligation clip applier FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery ligation clip applier

MICA Appliers by Vitalitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery ligation clip applier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitalitec International, Inc.

Sources (1)

  • FDA UDI ca05e94b-e602-4c74-a7b3-f2e4ed7227f4 35 fields · synced Jun 1, 2026