Rapid fFN

FFN Specimen Collection KIT, 25PK

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Zhejiang (2), Shanghai (1).

Chinese manufacturers registered for FDA product code LIO
Manufacturer City Province Registered as Device types
Zhejiang Gongdong Medical Technology Co., Ltd. Taizhou Zhejiang Contract manufacturer 40
Hangzhou Best Valley Medical Technology Co., Ltd. Hangzhou Zhejiang Exporter 20
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Record

Regulatory record for Rapid fFN
Listed by Hologic, Inc., United States
FDA product code LIO
Device type Device, Specimen Collection
Device class Class 1
Regulation 21 CFR 866.2900
Establishment Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K900225
Record published 2022-11-15

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 25 °C
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Rapid fFN
Catalogue number Size Per pack Status
FFN SPECIMEN COLLECTION KIT, 25PK 25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Remel Remel, Inc. 21
Sigma Virocult Medical Wire & Equipment Company (Bath), Ltd. 16
Transwab Medical Wire & Equipment Company (Bath), Ltd. 14
Puritan UniTranz-RT Puritan Medical Products Company LLC 13
Sigma Transwab Medical Wire & Equipment Company (Bath), Ltd. 11
Starswab II Bacteriology Culture Collection and Transport System Pretium Canada Packaging ULC 10
Vacuette Greiner BIO-ONE Gmbh 4
Bacti-Swab Remel, Inc. 4
Cardinal Health Cardinal Health 200, LLC 4
Puritan Puritan Medical Products Company LLC 4
Covidien Cardinal Health 200, LLC 3
Puritan Opti-Swab Puritan Medical Products Company LLC 3

Showing 12 of 35. All products under Device, Specimen Collection

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Rapid fFN
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Hologic, Inc. 510(k) number 2025-01-08 Class II Nonconforming Material/Component Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850) contain Rapid fFN Specimen Collection Tubes which may be empty, underfilled, or overfilled with extraction buffer. The transport tubes are used with the Fetal Fibr 1351 units

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer