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XeroGel

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
XeroGel FDA UDI
Generic Name
ENT space-occupying dressing, animal-derived FDA UDI
Device Name
Nasal Epistaxis 2 Pack FDA UDI
Model / Reference
XG-102 FDA UDI
Description
Nasal Epistaxis 2 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
10857326005533 FDA UDI
FDA Product Code
LYA FDA UDI
EMX 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
874.4100 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

Category: ENT space-occupying dressing, animal-derived

XeroGel 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 83e4c519-8e64-4682-92a2-a7a8fb0d2144 34 fields · synced Jun 8, 2026