biopsy forceps

FDA UDI

Class I (US FDA UDI)

by Suzhou AcuVu Medical Technology Co., Ltd.

Identity

Trade Name: biopsy forceps FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: Hysteroscopic surgical instruments are used for the removal of uterine lesions; the surgical instruments range from 1.66mm, 2.0mm and 2.3mm outside diameter; they are suitable for 5Fr, 6Fr and 7Fr hysteroscopes with working channel. FDA UDI
Model / Reference: RSI-340-5-C FDA UDI
Description: Hysteroscopic surgical instruments are used for the removal of uterine lesions; the surgical instruments range from 1.66mm, 2.0mm and 2.3mm outside diameter; they are suitable for 5Fr, 6Fr and 7Fr hysteroscopes with working channel. FDA UDI

Identifiers

Primary DI / UDI-DI: 06974880990246 FDA UDI
FDA Product Code: NWW FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.1690 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Atherectomy Cutter Diameter — 1.66 Millimeter FDA UDI
Atherectomy Cutter Diameter — 2 Millimeter FDA UDI
Atherectomy Cutter Diameter — 2.3 Millimeter FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

biopsy forceps by Suzhou AcuVu Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
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ELMED — ELMED INCORPORATED · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Suzhou AcuVu Medical Technology Co., Ltd.

Sources (1)

FDA UDI 7cd038f4-c8c9-4aa7-acc6-1afdb9fa4c48 36 fields · synced Jun 6, 2026