← Back to catalogue

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
The biopsy forceps are intended for use in hysteroscopy procedure to obtain tissue samples for examination of tissue from the uterine cavity. FDA UDI
Model / Reference
RSI-370-7-C FDA UDI
Description
The biopsy forceps are intended for use in hysteroscopy procedure to obtain tissue samples for examination of tissue from the uterine cavity. FDA UDI

Identifiers

Primary DI / UDI-DI
06974880993131 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization 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

Similar devices

Also classified as Rigid endoscopic biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e914e208-ee6e-490b-a298-fa2daff9aab5 35 fields · synced Jun 8, 2026