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PerClot

FDA UDI

Class III (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
PerClot FDA UDI
Generic Name
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI
Device Name
PerClot 1g - 9cm Standard Tip FDA UDI
Model / Reference
PCUS001 FDA UDI
Description
PerClot 1g - 9cm Standard Tip FDA UDI

Identifiers

Catalog Number
PCUS001 FDA UDI
Primary DI / UDI-DI
05413765891335 FDA UDI
PMA Number
P210036 FDA UDI
FDA Product Code
LMG FDA UDI
GMDN Term
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4490 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

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 Safe FDA UDI

Category: Plant polysaccharide haemostatic agent, bioabsorbable

PerClot by Baxter Healthcare Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Plant polysaccharide haemostatic agent, bioabsorbable.

Cleared under the same submission

P210036 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Baxter Healthcare Corp

Sources (1)

  • FDA UDI a13d4e8b-54d0-4fe0-ad61-73af5702e5af 36 fields · synced May 31, 2026