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Dr -hos

FDA UDI

Class II (US FDA UDI)

by Guangzhou Xinbo Electronic Co., Ltd.

Identity

Trade Name
DR -HOS FDA UDI
Generic Name
Mediastinal drainage catheter, non-antimicrobial FDA UDI
Device Name
Conductive Electrode Gel: a conductive medium for use on fabric or metal electrodes FDA UDI
Model / Reference
DHGEL FDA UDI
Description
Conductive Electrode Gel: a conductive medium for use on fabric or metal electrodes FDA UDI

Identifiers

Primary DI / UDI-DI
06970742221671 FDA UDI
510(k) Number
K200402 FDA UDI
FDA Product Code
GYB FDA UDI
GMDN Term
Mediastinal drainage catheter, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Mediastinal drainage catheter, non-antimicrobial

Dr -hos by Guangzhou Xinbo Electronic Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mediastinal drainage catheter, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Guangzhou Xinbo Electronic Co., Ltd.

Sources (1)

  • FDA UDI 66a5e812-8a24-4ae3-b859-249aefada989 34 fields · synced Jun 8, 2026