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Quicktrach II

FDA UDI

Class II (US FDA UDI)

by VBM Medizintechnik GmbH

Identity

Trade Name
Quicktrach II FDA UDI
Generic Name
Cricothyrotomy kit, single-use FDA UDI
Model / Reference
30-10-904-1 FDA UDI

Identifiers

Primary DI / UDI-DI
04250105629989 FDA UDI
510(k) Number
K874742 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Cricothyrotomy kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 4 Millimeter FDA UDI

Category: Cricothyrotomy kit, single-use

Quicktrach II by VBM Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cricothyrotomy kit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 71ee1d22-1c57-4b43-bf11-7a38fcab1cbc 36 fields · synced May 30, 2026