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Marpac Inc

FDA UDI

Class I (US FDA UDI)

by Marpac, Inc.

Identity

Trade Name
Marpac Inc FDA UDI
Generic Name
Tracheostomy tube neck holder, single-use FDA UDI
Device Name
Pediatric trach tube holder, one-piece, with twill ties FDA UDI
Model / Reference
107 FDA UDI
Description
Pediatric trach tube holder, one-piece, with twill ties FDA UDI

Identifiers

Primary DI / UDI-DI
00653658001075 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Tracheostomy tube neck holder, single-use 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tracheostomy tube neck holder, single-use

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

Similar devices

Also classified as Tracheostomy tube neck holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marpac, Inc.

Sources (1)

  • FDA UDI 8513fba0-6b8d-4c6c-a8af-c946b3bb6509 34 fields · synced Jun 6, 2026