What is FDA product code OIJ?

FDA has exempted these devices from the premarket notification requirement by publishing in the Federal Register of July 11, 2017 (82 FR 31976) available at https://www.federalregister.gov/documents/2017/07/11/2017-14453/medical-devices-exemptions-from-premarket-notification-class-ii-devices subject to the limitations under 21 CFR XXX.9, where XXX refers to Parts 862-892, and any limitations on the exemption described in (82 FR 31976). Any device that exceeds the limitations found in 21 CFR sections 862.9 to 892.9 or identified in the Federal Register (82 FR 31976) available at https://www.federalregister.gov/documents/2017/07/11/2017-14453/medical-devices-exemptions-from-premarket-notification-class-ii-devices is required to submit a premarket notification submission (510(k)) to FDA before introducing a device into interstate commerce. If a manufacturers device is exempt from the pr

Radiology › DiagnosticBiopsy Needle Guide Kit

iSR’obot Kit

Name: iSR'obot Kit
Brand: iSR'obot Kit

4 catalogue numbers from iSR'obot Kit - 13G, listed by Biobot Surgical Pte. Ltd., Singapore, under Biopsy Needle Guide Kit. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26

4manufacturers in China registered for this device type

4catalogue numbers in this listing

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code OIJ
Manufacturer	City	Province	Registered as	Device types
Well Lead Medical Co., Ltd.	Guangzhou	Guangdong	Contract manufacturer	46
Sonoscape Medical Corp.	Shenzhen	Guangdong	Manufacturer	7
Shenzhen Wisonic Medical Technology Co., Ltd.	Shenzhen	Guangdong	Manufacturer	4
Jingfang Precision Medical Device(Shenzhen) Co., Ltd.	Shenzhen	Guangdong	Manufacturer	1

Record

Regulatory record for iSR’obot Kit
Listed by	Biobot Surgical Pte. Ltd., Singapore
FDA product code	OIJ
Device type	Biopsy Needle Guide Kit
Device class	Class 2
Regulation	21 CFR 892.1560
Establishment	Manufacturer
510(k)	K232320
Record published	2024-06-14
Record revised	2024-06-14 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Supplied sterile	Yes
Single use	Yes
Supplied as a kit	Yes
Label carries	lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for iSR’obot Kit
Catalogue number	Size	Status
iSR’obot Kit – 13G		In distribution
iSR’obot Kit – 14G		In distribution
iSR’obot Kit – 17G		In distribution
iSR’obot Kit – 18G		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
InnoFine	Jingfang Precision Medical Device(Shenzhen) Co., Ltd.	531
SonoScape	Sonoscape Medical Corp.	70
Hitachi	Hitachi, Ltd.	57
Mindray	Jingfang Precision Medical Device(Shenzhen) Co., Ltd.	16
Sheathes	Sheathing Technologies, Inc.	14
Cardinal Health	Cardinal Health 200, LLC	12
Sheathes3D	Sheathing Technologies, Inc.	7
NGB-007 Needle-guided Bracket	Shenzhen Mindray BIO-Medical Electronics Co., Ltd.	2
NGB-011 Needle-guided Bracket	Shenzhen Mindray BIO-Medical Electronics Co., Ltd.	2
NGB-022 Needle-guided Bracket	Shenzhen Mindray BIO-Medical Electronics Co., Ltd.	2
NGB-018 Needle-guided Bracket	Shenzhen Mindray BIO-Medical Electronics Co., Ltd.	2
Moving-Shot Guide	RF Medical Co., Ltd.	2

Showing 12 of 45. All products under Biopsy Needle Guide Kit

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.