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Tube holder

FDA UDI

Class I (US FDA UDI)

by Reison Medical AB

Identity

Trade Name
Tube holder FDA UDI
Generic Name
Breathing circuit tube holder FDA UDI
Model / Reference
10-610 FDA UDI

Identifiers

Primary DI / UDI-DI
07350111832698 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Breathing circuit tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Category: Breathing circuit tube holder

Tube holder by Reison Medical AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reison Medical AB

Sources (1)

  • FDA UDI b3c1b07e-65d3-4f92-8aae-ed3805cfb767 32 fields · synced Jun 6, 2026