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HV Heart Retractor Handle

FDA UDI

Class I (US FDA UDI)

by USB Medical, Ltd.

Identity

Trade Name
HV Heart Retractor Handle FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
USB Heart Retractor Handle FDA UDI
Model / Reference
HVR-H1 FDA UDI
Description
USB Heart Retractor Handle FDA UDI

Identifiers

Catalog Number
HVR-H1 FDA UDI
Primary DI / UDI-DI
00850037179084 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

No

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

HV Heart Retractor Handle 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 de6ae407-ab99-4841-b7d7-93dd13d74e2a 34 fields · synced May 30, 2026