What is FDA product code OIE?

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. 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.

Hematology › Pathology InstrumentationUrine Collection Kit (Excludes Hiv Testing)

Progensa

Name: Progensa
Brand: Progensa

Catalogue number PCA3 URINE TRANSPORT, listed by Hologic, Inc., United States, under Urine Collection Kit (Excludes Hiv Testing). 7 manufacturers in China are registered for this product code.

Registry build 21.09.26

7manufacturers in China registered for this device type

1catalogue number

1recall

Who Else Makes It

Concentrated in Zhejiang (3), Jiangsu (2), Guangdong (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OIE
Manufacturer	City	Province	Registered as	Device types
Conod Medical Co., Limited	Changshu	Jiangsu	Contract manufacturer	48
Zhejiang Gongdong Medical Technology Co., Ltd.	Taizhou	Zhejiang	Contract manufacturer	40
Primecare Medical (Suzhou) Co., Ltd.	Changshu	Jiangsu	Contract manufacturer	20
Principle & Will Biotech (Pinghu) Co., Ltd.	Pinghu	Zhejiang	Contract manufacturer	39
Hangzhou Primecare Medical Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	29
Phase Scientific (Shenzhen) Company Limited	Shenzhen	Guangdong	Repacker / relabeller	8
Equinox Biotech Co., Ltd.	Shantou	Guangdong	Manufacturer	5

Record

Regulatory record for Progensa
Listed by	Hologic, Inc., United States
FDA product code	OIE
Device type	Urine Collection Kit (Excludes Hiv Testing)
Device class	Class 1
Regulation	21 CFR 864.3250
Establishment	Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published	2014-09-17
Record revised	2024-05-20 (version 4)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Single use	Yes
Prescription	Prescription only
Supplied as a kit	Yes
Label carries	lot or batch number, expiry date
Distribution end date	2021-11-30
UDI direct marking	Exempt

Catalogue Numbers

Catalogue numbers for Progensa
Catalogue number	Size	Per pack	Status
PCA3 URINE TRANSPORT		50	Withdrawn

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Medical Action Industries	Medical Action Industries, Inc.	15
Medline	Medline Industries, Inc.	4
Vacuette	Greiner BIO-ONE Gmbh	4
Recopad	Medfire Innovations Inc.	3
Smilereader ovulation test kit	Equinox Biotech Co., Ltd.	3
David	Equinox Biotech Co., Ltd.	3
Everlywell Urine Collection Kit	Everly Health, Inc.	2
Urine Raku-Ryu Cup	Takahashi Keisei Corporation	2
Therapak	Therapak, LLC	2
BD Vacutainer Urine Complete Cup Kit	Becton, Dickinson AND Company	2
SureStep Vacutainer Urine Sampling Kit	C.R. Bard, Inc.	2
LotFancy	Equinox Biotech Co., Ltd.	1

Showing 12 of 32. All products under Urine Collection Kit (Excludes Hiv Testing)

Recalls

1 of these is Class III. 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
2014-04-17	Class III	Labeling mix-ups	Incorrect labeling was used on each pouch of the affected lots of APTIMA Urine Specimen Collection Kits. The outer box of the kits are identified correctly as “APTIMA Urine Collection Kits”; however, the inner pouches are incorrectly labele	4,740 units	2014-08-26

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.