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Dr Zee

FDA UDI

Class I (US FDA UDI)

by Resp Devices LLC

Identity

Trade Name
Dr Zee FDA UDI
Generic Name
Tracheostomy tube neck holder, single-use FDA UDI
Device Name
Tracheostomy Tube Holders. Two-Piece Wick Foam Collar with Hook and Loop Closure, Neonatal/Infant, 10/bx FDA UDI
Model / Reference
8015 FDA UDI
Description
Tracheostomy Tube Holders. Two-Piece Wick Foam Collar with Hook and Loop Closure, Neonatal/Infant, 10/bx FDA UDI

Identifiers

Catalog Number
8015 FDA UDI
Primary DI / UDI-DI
00850043061069 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

Yes

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

Dr Zee by Resp Devices LLC — 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
Resp Devices LLC

Sources (1)

  • FDA UDI f62aa899-553a-4eee-8cde-524898843dad 37 fields · synced May 30, 2026