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EndoClot

FDA UDI

Class II (US FDA UDI)

by EndoClot Plus, Inc.

Identity

Trade Name
EndoClot FDA UDI
Generic Name
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI
Device Name
EndoClot®Polysaccharide Hemostatic System, EndoClot® PHS FDA UDI
Model / Reference
EPK2302-01 FDA UDI
Description
EndoClot®Polysaccharide Hemostatic System, EndoClot® PHS FDA UDI

Identifiers

Primary DI / UDI-DI
16972011720011 FDA UDI
510(k) Number
K190677 FDA UDI
FDA Product Code
QAU FDA UDI
GMDN Term
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4456 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Plant polysaccharide haemostatic agent, bioabsorbable

EndoClot by EndoClot Plus, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Plant polysaccharide haemostatic agent, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EndoClot Plus, Inc.

Sources (1)

  • FDA UDI 572be470-df59-4bec-8bdf-01b1b1c017c9 34 fields · synced May 30, 2026