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Hsiner

FDA UDI

Class I (US FDA UDI)

by Hsiner Company

Identity

Trade Name
Hsiner FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Corrugate Catheter Mount, tubing length: 15cm, 22OD/15ID; 22ID FDA UDI
Model / Reference
1 FDA UDI
Description
Corrugate Catheter Mount, tubing length: 15cm, 22OD/15ID; 22ID FDA UDI

Identifiers

Catalog Number
VY70134-22F FDA UDI
Primary DI / UDI-DI
04711064686760 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Hsiner by Hsiner Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hsiner Company

Sources (1)

  • FDA UDI ff3253dc-74a7-47b1-bbda-336af050b0f4 34 fields · synced May 30, 2026