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Closed Suction System for Adult

FDA UDI

Class I (US FDA UDI)

by Vr Medical Technology

Identity

Trade Name
Closed Suction System for Adult FDA UDI
Generic Name
Tracheostomy tube cuff FDA UDI
Model / Reference
VR04214US FDA UDI

Identifiers

Primary DI / UDI-DI
06959180703727 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Tracheostomy tube cuff FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tracheostomy tube cuff

Closed Suction System for Adult by Vr Medical Technology — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa01166f-c085-4f40-88f9-cb8dc22baca1 32 fields · synced May 30, 2026