# Arrow IPN927039

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/arrow-ask-32041-lmdtg>
- Manufacturer: [Teleflex Incorporated](https://devicerts.com/manufacturers/teleflex-incorporated) (FDA registration: United States)
- Name in the registry: ARROW IPN927039
- Device class: Class II (US FDA)
- FDA product code: PND
- GMDN: Peripheral intravenous catheterization kit, non-sensing (64573)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 10801902213065 · listed 2024-08-01 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K213855 · decision 2022-09-02 · decision SESE · status: Active · from GUDID

## Recalls

- Z-2387-2026 · Class I · ongoing · initiated 2026-04-21: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

## Identity

- Trade name: ARROW [FDA GUDID (AccessGUDID)]
- Generic name: Peripheral intravenous catheterization kit, non-sensing [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: IPN927039 [FDA GUDID (AccessGUDID)]; ASK-32041-LMDTG [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 10801902213065 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K213855 [FDA GUDID (AccessGUDID)]
- FDA product code: PND [FDA GUDID (AccessGUDID)]
- GMDN term: Peripheral intravenous catheterization kit, non-sensing (64573) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 880.5200 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- MRI safety: MR Safe [FDA GUDID (AccessGUDID)]

## Properties

- Supplied sterile: Yes [FDA GUDID (AccessGUDID)]
- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Convenience kit: Yes [FDA GUDID (AccessGUDID)]
- Combination product: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [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)]
- 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: Arrow IPN927039, Teleflex Incorporated. deviCERTS medical device catalogue. https://devicerts.com/devices/arrow-ask-32041-lmdtg (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/arrow-ask-32041-lmdtg.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/arrow-ask-32041-lmdtg
- 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.