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Tube set for suction, single-use

FDA UDI

Class II (US FDA UDI)

by W.O.M. World of Medicine GmbH

Identity

Trade Name
Tube set for suction, single-use FDA UDI
Generic Name
Disposable vacuum tubing FDA UDI
Model / Reference
OTFLWTBING2 FDA UDI

Identifiers

Primary DI / UDI-DI
04056702008819 FDA UDI
FDA Product Code
HIG FDA UDI
HET FDA UDI
GMDN Term
Disposable vacuum tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1700 FDA UDI
884.1720 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Disposable vacuum tubing

Tube set for suction, single-use by W.O.M. World of Medicine GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Disposable vacuum tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c86aa1e2-1955-4c63-8177-049f35f2810e 32 fields · synced May 30, 2026