Finetouch

LANCET

Description
TERUMO FINETOUCH® lancet for use exclusively with the TERUMO FINETOUCH® lancing device.

Intended use
This product is designed to collect capillary blood from the fingertip, earlobe, or heel using the dedicated TERUMO FINETOUCH® device.

Classification
CE 0197 - MDD 93/42/EEC – class IIa – Italian Legislative Decree 46/97.

Compliance
Total Quality System EN ISO 9001:2008, EN ISO 13485:2003/AC:2009, Compliant specifications: EN 980:2008, EN 1041:2008, EN ISO 780:1999, EN ISO 14971:2009, EN 62366:2008, EN ISO 11137-1:2006, EN ISO 11137-2:2007/AC:2009, EN 556-1:2001/AC:2006, EN ISO 11607-1:2009, EN ISO 11607-2:2006, EN ISO 11737- 1:2006/AC:2009, EN ISO 11737-2:2009, EN ISO 10993-1:2009/AC:2010, EN ISO 10993-4:2009, EN ISO 10993-5:2009, EN ISO 10993-10:2009, EN ISO 10993-11:2009, EN ISO 10993-12:2009, EN ISO 10993-18:2009, EP 2.6.1 (2008).

Features
- Terumo hollow needle (23G) with triple bevel cut.
- The lancet design prevents the risk of accidental needle sticks.
- The needle is protected by the lancet's safety device before and after use.
- The lancet cannot be reused.
- The lancet design protects the lancing device from contact with patients' skin or blood, preventing cross-contamination.
- Rigid individual packaging.
- Virtually painless.
- Validity 36 months.
- Gamma ray sterilization in accordance with relevant European Standards.
- Sterile.
- Single use.

Code MS*GN4525G