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Relieva Circa

FDA UDI

Class I (US FDA UDI)

by Acclarent, Inc.

Identity

Trade Name
RELIEVA CIRCA FDA UDI
Generic Name
Bone-coring punch, single-use FDA UDI
Device Name
RELIEVA CIRCA ETHMOID PUNCH FDA UDI
Model / Reference
EP01 FDA UDI
Description
RELIEVA CIRCA ETHMOID PUNCH FDA UDI

Identifiers

Catalog Number
EP01 FDA UDI
Primary DI / UDI-DI
10705031230989 FDA UDI
FDA Product Code
KAX FDA UDI
GMDN Term
Bone-coring punch, single-use 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone-coring punch, single-use

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

Similar devices

Also classified as Bone-coring punch, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acclarent, Inc.

Sources (1)

  • FDA UDI 2c78043d-d95a-4042-99c8-10180172c2ef 36 fields · synced May 30, 2026