NF EN ISO 21533

NF EN ISO 21533

February 2004
Standard Cancelled

Dentistry - Reusable cartridge syringes intented for intraligamentary injections

ISO 21533:2003 specifies requirements and test methods for reusable cartridge syringes intended for intraligamentary injections.It specifies requirements for dental cartridge syringes only with ISO metric thread sizes, and only intended for intraligamentary injections. However, imperial thread sizes are considered in an informative annex.

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Main informations

Collections

National standards and national normative documents

Publication date

February 2004

Number of pages

14 p.

Reference

NF EN ISO 21533

ICS Codes

11.040.20   Transfusion, infusion and injection equipment
11.060.25   Dental instruments

Classification index

S91-184

Print number

1 - 04/05/2004

International kinship

European kinship

EN ISO 21533:2003
Sumary
Dentistry - Reusable cartridge syringes intented for intraligamentary injections

ISO 21533:2003 specifies requirements and test methods for reusable cartridge syringes intended for intraligamentary injections.

It specifies requirements for dental cartridge syringes only with ISO metric thread sizes, and only intended for intraligamentary injections. However, imperial thread sizes are considered in an informative annex.

Standard replaced by (1)
NF EN ISO 21533
January 2018
Standard Current
Dentistry - Reprocessable cartridge syringes for intraligamentary injections

ISO 21533:2018 specifies requirements and test methods for reprocessable cartridge syringes intended for intraligamentary injections. ISO 21533:2018 specifies requirements for cartridge syringes with ISO metric thread sizes, and only intended for intraligamentary injections. However, attention is drawn to the existence of a variety of syringes with imperial thread sizes (see Annex A).

Table of contents
  • Avant-propos
    iv
  • 1 Domaine d'application
    1
  • 2 Références normatives
    1
  • 3 Termes et définitions
    1
  • 4 Exigences
    2
  • 4.1 Conception
    2
  • 4.2 Corps
    3
  • 4.3 Embout fileté pour le montage de l'aiguille
    3
  • 4.4 Tige poussoir
    3
  • 4.5 Volume d'anesthésique local expulsé
    3
  • 4.6 Résistance à la corrosion, au passage à l'autoclave et à l'exposition à la chaleur
    3
  • 5 Méthodes d'essai
    4
  • 5.1 Examen visuel
    4
  • 5.2 Mesurage du volume expulsé
    4
  • 5.3 Déplacement de la tige poussoir
    4
  • 5.4 Détachement de l'étui protecteur
    4
  • 5.5 Essai à l'eau bouillante
    4
  • 5.6 Essai de passage à l'autoclave
    4
  • 5.7 Essai d'exposition à la chaleur sèche
    4
  • 6 Notice du fabricant
    4
  • 7 Marquage
    5
  • 7.1 Marquage de l'emballage unitaire
    5
  • 7.2 Marquage de la seringue
    5
  • Annexe A (informative) Filetages en inches
    6
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