# Aimstrip Us-5B 55200

> Listed: FDA GUDID listing, no authorization on record. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/aimstrip-us-5b-55200>
- Manufacturer: [Germaine Laboratories, Inc.](https://devicerts.com/manufacturers/fda-fei-3001451797) (FDA registration: United States)
- Name in the registry: AIMSTRIP US-5B 55200
- Device class: Class I (US FDA)
- FDA product code: LJX, KQO, JRE, JMT, JIR, JIO, JIL
- GMDN: Multiple urine analyte IVD, kit, rapid colorimetric, clinical (54514)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00695684552008 · listed 2016-04-27 · status: Listed (GUDID: in commercial distribution)

## Recalls

No recall on record.

## Identity

- Trade name: AIMSTRIP US-5B [FDA GUDID (AccessGUDID)]
- Generic name: Multiple urine analyte IVD, kit, rapid colorimetric, clinical [FDA GUDID (AccessGUDID)]
- Model / reference: 55200 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00695684552008 [FDA GUDID (AccessGUDID)]
- FDA product code: LJX [FDA GUDID (AccessGUDID)]; KQO [FDA GUDID (AccessGUDID)]; JRE [FDA GUDID (AccessGUDID)]; JMT [FDA GUDID (AccessGUDID)]; JIR [FDA GUDID (AccessGUDID)]; JIO [FDA GUDID (AccessGUDID)]; JIL [FDA GUDID (AccessGUDID)]
- GMDN term: Multiple urine analyte IVD, kit, rapid colorimetric, clinical (54514) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class I [FDA GUDID (AccessGUDID)]
- Regulation number: 864.7675 [FDA GUDID (AccessGUDID)]; 862.2900 [FDA GUDID (AccessGUDID)]; 862.2800 [FDA GUDID (AccessGUDID)]; 862.1510 [FDA GUDID (AccessGUDID)]; 862.1645 [FDA GUDID (AccessGUDID)]; 864.6550 [FDA GUDID (AccessGUDID)]; 862.1340 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Aimstrip Us-5B 55200, Germaine Laboratories, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/aimstrip-us-5b-55200 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/aimstrip-us-5b-55200.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/aimstrip-us-5b-55200
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.