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USB HV Heart Retractor Blade Set

FDA UDI

Class I (US FDA UDI)

by USB Medical, Ltd.

Identity

Trade Name
USB HV Heart Retractor Blade Set FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
Re-usable blades used with the HV heart retractor for use in minimally invasive surgical procedures contains: DF-101 Delivery Forceps, 6 each Mitral Blades & HVR-T2 Large Sterilization Tray FDA UDI
Model / Reference
HVB-06 FDA UDI
Description
Re-usable blades used with the HV heart retractor for use in minimally invasive surgical procedures contains: DF-101 Delivery Forceps, 6 each Mitral Blades & HVR-T2 Large Sterilization Tray FDA UDI

Identifiers

Catalog Number
HVB-06 FDA UDI
Primary DI / UDI-DI
00850037179749 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held surgical retractor, reusable

USB HV Heart Retractor Blade Set by USB Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
USB Medical, Ltd.

Sources (1)

  • FDA UDI 7908e21f-d932-494b-bf54-7c45c2dd9064 34 fields · synced Jun 6, 2026