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Hemopore

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Hemopore FDA UDI
Generic Name
ENT space-occupying dressing, animal-derived FDA UDI
Model / Reference
5400020208 FDA UDI

Identifiers

Catalog Number
5400-020-208 FDA UDI
Primary DI / UDI-DI
07613327117233 FDA UDI
FDA Product Code
LYA FDA UDI
GMDN Term
ENT space-occupying dressing, animal-derived FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4780 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 8.0 Centimeter FDA UDI

Category: ENT space-occupying dressing, animal-derived

Hemopore by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT space-occupying dressing, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 679cbaa3-fa5a-439c-84af-0d6d921603f4 36 fields · synced May 30, 2026