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Jiyuan

FDA UDI

Class I (US FDA UDI)

by Jiangsu Jiyuan Medical Technology Co., Ltd

Identity

Trade Name
Jiyuan FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, single-use FDA UDI
Device Name
Coarse-tooth type, 350mm, diameter 1.5mm, FDA UDI
Model / Reference
JY-CC-350-15-S FDA UDI
Description
Coarse-tooth type, 350mm, diameter 1.5mm, FDA UDI

Identifiers

Primary DI / UDI-DI
06973672290427 FDA UDI
FDA Product Code
HFB FDA UDI
GMDN Term
Rigid endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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

Yes

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: Rigid endoscopic biopsy forceps, single-use

Jiyuan by Jiangsu Jiyuan 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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75b5fdbd-2fdf-4578-aa6d-b016736c2d1c 34 fields · synced May 30, 2026