What is FDA product code LRS?

This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Regard™ · I.V. Start Kit → General Hospital

Name: Regard™
Brand: Regard™

7manufacturers in China registered for this device type

6catalogue numbers in this listing

2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Hubei (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LRS
Manufacturer	City	Province	Registered as	Device types
Conod Medical Co., Limited	Changshu	Jiangsu	Contract manufacturer	48
Jiangsu NEW Pentastar Medical Products Co., Ltd.	Changzhou	Jiangsu	Exporter	146
Amsino Medical (Kunshan) Co., Ltd.	Kunshan	Jiangsu	Contract manufacturer	53
Hubei Lanbin Medical Group Co., Ltd.	Xiaogan	Hubei	Contract manufacturer	33
Zibo Qichuang Medical Products Co., Ltd.	Zibo	Shandong	Manufacturer	27
Yafho BIO-Technology Co., Ltd.	Guangzhou	Guangdong	Manufacturer	14
Xiamen ANK Hygiene Care Product Co., Ltd.	Xiamen	Fujian	Manufacturer	11

Record

Regulatory record for Regard™
Listed by	ROi CPS LLC
FDA product code	LRS
Device type	I.V. Start Kit
Device class	Class 2
Regulation	21 CFR 880.5200
Premarket notification	Exempt
Record published	2021-07-22
Record revised	2025-04-14 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Supplied sterile	Yes
Single use	Yes
Prescription	Prescription only
Supplied as a kit	Yes
Label carries	lot or batch number, expiry date
Packaging	Pack of 50, pack of 10
Distribution end date	2025-04-11

Catalogue Numbers

Catalogue numbers for Regard™
Catalogue number	Size	Status
IV01121B		Withdrawn
IV01121		Withdrawn
IV01121D		Withdrawn
IV01121A		Withdrawn
IV01159		Withdrawn
IV01121C		Withdrawn

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Cardinal Health	Cardinal Health 200, LLC	1,066
Centurion	Centurion Medical Products Corporation	886
Medline Industries, Inc.	Medline Industries, Inc.	740
Medline	Medline Industries, Inc.	621
Medical Action Industries	Medical Action Industries, Inc.	512
Curaplex	Bound Tree Medical, LLC	149
Motion Medical Distributing	Haslam Medical, Inc.	118
LSL Healthcare	Lsl Industries, Inc.	83
Vygon	Vygon Corp.	76
Trinity Sterile, Inc.	Trinity Sterile, Inc.	63
MediChoice	Owens & Minor Distribution, Inc.	46
McKesson	Mckesson Medical-Surgical Inc.	21

Showing 12 of 58. All products under I.V. Start Kit

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated	FDA class	Root cause	Reason	Quantity	Closed
2022-03-18	Class II	Nonconforming Material/Component	A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation of test methods used in its manufacture.	950 convenience kits	2024-08-02
2022-02-24	Class III	Material/Component Contamination	Recalled devices were packaged in convenience kits.	1750 kits	2022-04-25

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.

Regard™