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InnoFine

FDA UDI

Class II (US FDA UDI)

by JingFang Precision Medical Device(Shenzhen) Co., Ltd.

Identity

Trade Name
InnoFine FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
Disposable Needle Guides for transperineal biopsy, used with Mindray ELC13-4U, ELC13-4s Ultrasound Transducers FDA UDI
Model / Reference
DT-006 FDA UDI
Description
Disposable Needle Guides for transperineal biopsy, used with Mindray ELC13-4U, ELC13-4s Ultrasound Transducers FDA UDI

Identifiers

Catalog Number
11090 FDA UDI
Primary DI / UDI-DI
06975122550907 FDA UDI
FDA Product Code
OIJ FDA UDI
GMDN Term
Needle guide, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 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

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: Needle guide, single-use

InnoFine by JingFang Precision Medical Device(Shenzhen) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 773fda77-b6b8-426f-a941-698be63e2d26 36 fields · synced Jun 6, 2026