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Relieva Spin

FDA UDI

Class I (US FDA UDI)

by Acclarent, Inc.

Identity

Trade Name
RELIEVA SPIN FDA UDI
Generic Name
Nasal haemostatic balloon FDA UDI
Device Name
RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT, 1 PK FDA UDI
Model / Reference
RS0616MZ FDA UDI
Description
RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT, 1 PK FDA UDI

Identifiers

Catalog Number
RS0616MZ FDA UDI
Primary DI / UDI-DI
20705031200576 FDA UDI
510(k) Number
K111875 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 Spin 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 2d6b677c-9f86-490b-b4c0-37d549958ae5 37 fields · synced May 30, 2026