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Low-pressurehose assembly, 2m, 02 green DISS/ OHMEDA

FDA UDI

Class II (US FDA UDI)

by Weinmann Emergency Medical Technology GmbH + Co. KG

Identity

Trade Name
Low-pressurehose assembly, 2m, 02 green DISS/ OHMEDA FDA UDI
Generic Name
General-gas low pressure tubing, reusable FDA UDI
Model / Reference
36336 FDA UDI

Identifiers

Primary DI / UDI-DI
04054685271619 FDA UDI
510(k) Number
K193191 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
General-gas low pressure tubing, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-gas low pressure tubing, reusable

Low-pressurehose assembly, 2m, 02 green DISS/ OHMEDA by Weinmann Emergency Medical Technology GmbH + Co. KG — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as General-gas low pressure tubing, reusable.

Cleared under the same submission

K193191 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Weinmann Emergency Medical Technology GmbH + Co. KG

Sources (1)

  • FDA UDI 1d52829c-c3fb-4bf7-ae3d-7fa1c22374e3 33 fields · synced May 30, 2026