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Provox LaryClip

FDA UDI

Class I (US FDA UDI)

by Atos Medical Inc.

Identity

Trade Name
Provox LaryClip FDA UDI
Generic Name
Tracheostomy tube neck holder, reusable FDA UDI
Device Name
The Provox LaryClip is used for extra support for LaryButton and LaryTube. The product consists of two parts, one that is attached to the patients’ skin on each side of the stoma and the other part is attached to the LaryButton or the LaryTube. The two parts are then connected by Velcro. FDA UDI
Model / Reference
7669 FDA UDI
Description
The Provox LaryClip is used for extra support for LaryButton and LaryTube. The product consists of two parts, one that is attached to the patients’ skin on each side of the stoma and the other part is attached to the LaryButton or the LaryTube. The two parts are then connected by Velcro. FDA UDI

Identifiers

Catalog Number
7669 FDA UDI
Primary DI / UDI-DI
07331791002687 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Tracheostomy tube neck holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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: Tracheostomy tube neck holder, reusable

Provox LaryClip by Atos Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube neck holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atos Medical Inc.

Sources (1)

  • FDA UDI 7325c35e-bf05-47d8-b14e-44dbda3ee774 36 fields · synced May 31, 2026