AMIES with CHARCOAL - Polystyrene + viscose

Organization name

Deltalab, S.L.

SRN

ES-MF-000000153

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW010

  1. If it appears that the unitary packaging has lost its integrity, do not use the swab as there is no guarantee of its sterility. 2. Do not use in case of missing component or the product information is not displayed correctly. 3. Discard the product if you find any broken, dirt, chipped, loose tips and/or tipless swab. 4. Do not use if expiry date has been overcome. 5. Do not use if alteration is observed in the transport medium. 6. Do not ingest the transport medium under any circumstances. 7. For single use. The reuse of this product may cause infections. 8. Handle carefully. Any strong pressure during use, although unlikely, could break the swab. In case of damage, discard immediately. 10. Not suitable for any other application than its intended use. 11. For pediatric use it is recommended to use swabs with plastic handle. 12. The use of the swab presents no difficulty for the intended end users. 13. After use, the swabs must be decontaminated or treated as contaminated medical waste. It is the responsibility of each laboratory to handle, treat and dispose the waste according to the regulations. Unused swabs can be considered non-hazardous products and can be disposed of accordingly. 14. The swabs with transport medium include instructions with diagrams for use on the primary package (peel-pouch)

Primary placement in Poland; available across 1 country total.

Trade name

AMIES with CHARCOAL - Polystyrene + viscose

UDI-DI code

08435263873078

Basic UDI-DI

84356058UDI-DI-005W

Reference / catalog number

7012211110

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

6

Additional product description

—

Additional information URL

https://www.deltalabgroup.com/eifus

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• A1102SAMPLE COLLECTION SWABS WITH TRANSPORT MEDIUM

Certificate health across this manufacturer's portfolio.