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NovaLine

FDA UDI

Class II (US FDA UDI)

by Bain Medical Equipment (Guangzhou) Co., Ltd.

Identity

Trade Name
NovaLine FDA UDI
Generic Name
Haemodialysis system transducer protector FDA UDI
Model / Reference
956007 FDA UDI

Identifiers

Primary DI / UDI-DI
06948082770036 FDA UDI
510(k) Number
K240164 FDA UDI
FDA Product Code
FIB FDA UDI
GMDN Term
Haemodialysis system transducer protector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

Yes

FDA UDI

Category: Haemodialysis system transducer protector

NovaLine by Bain Medical Equipment (Guangzhou) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system transducer protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bc742baf-5a73-45b9-9142-8f2a157afb04 33 fields · synced May 30, 2026