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Relieva Spinplus

FDA UDI

Class I (US FDA UDI)

by Acclarent, Inc.

Identity

Trade Name
RELIEVA SPINPLUS FDA UDI
Generic Name
Nasal haemostatic balloon FDA UDI
Device Name
RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT FDA UDI
Model / Reference
RSP0616F FDA UDI
Description
RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT FDA UDI

Identifiers

Catalog Number
RSP0616F FDA UDI
Primary DI / UDI-DI
10705031232914 FDA UDI
510(k) Number
K143541 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Nasal haemostatic balloon FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

Yes

FDA UDI

Category: Nasal haemostatic balloon

Relieva Spinplus by Acclarent, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal haemostatic balloon.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acclarent, Inc.

Sources (1)

  • FDA UDI f49906ba-dfae-4451-ba3f-1ebf007aca30 37 fields · synced Jun 8, 2026