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Rhino Rocket

FDA UDI

Class I (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
Rhino Rocket FDA UDI
Generic Name
Intranasal splint, non-bioabsorbable, animal-derived FDA UDI
Device Name
Sterile Expandacell Sponge, Wideline Nasal Pack, Medium (polyvinyl alcohol sponge) (6/PK) FDA UDI
Model / Reference
70890729 FDA UDI
Description
Sterile Expandacell Sponge, Wideline Nasal Pack, Medium (polyvinyl alcohol sponge) (6/PK) FDA UDI

Identifiers

Primary DI / UDI-DI
00821925037069 FDA UDI
FDA Product Code
EMX FDA UDI
GMDN Term
Intranasal splint, non-bioabsorbable, animal-derived FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Category: Intranasal splint, non-bioabsorbable, animal-derived

Rhino Rocket by Gyrus Acmi, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-bioabsorbable, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gyrus Acmi, Inc.

Sources (1)

  • FDA UDI 560ac978-19f9-49af-9cee-2bb568645a9b 33 fields · synced Jun 8, 2026