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Manta

FDA UDI

Class III (US FDA UDI)

by Essential Medical, Inc.

Identity

Trade Name
MANTA FDA UDI
Generic Name
Femoral artery closure plug/patch, collagen FDA UDI
Device Name
14F MANTA Vascular Closure Device FDA UDI
Model / Reference
2156 FDA UDI
Description
14F MANTA Vascular Closure Device FDA UDI

Identifiers

Primary DI / UDI-DI
00856279007079 FDA UDI
FDA Product Code
MGB FDA UDI
GMDN Term
Femoral artery closure plug/patch, collagen FDA UDI

Classification

Device Class
Class III 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

No

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
MRI Safety
MR Conditional FDA UDI

Category: Femoral artery closure plug/patch, collagen

Manta by Essential Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral artery closure plug/patch, collagen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Essential Medical, Inc.

Sources (1)

  • FDA UDI 3e814640-c47e-482f-8c87-7345fc76cba5 34 fields · synced May 30, 2026