ASTM F1026-1986(2008) Standard Specification for General Workmanship and Performance Measurements of Hemostatic Forceps.pdf
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1、Designation: F 1026 86 (Reapproved 2008)Standard Specification forGeneral Workmanship and Performance Measurements ofHemostatic Forceps1This standard is issued under the fixed designation F 1026; the number immediately following the designation indicates the year oforiginal adoption or, in the case
2、of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1. Scope1.1 This specif
3、ication covers general workmanship aspectsof hemostatic forceps fabricated from stainless steel andintended for reuse in surgery.2. Referenced Documents2.1 ASTM Standards:2E18 Test Methods for Rockwell Hardness of MetallicMaterialsE92 Test Method for Vickers Hardness of Metallic Mate-rialsE 140 Hard
4、ness Conversion Tables for Metals RelationshipAmong Brinell Hardness, Vickers Hardness, RockwellHardness, Superficial Hardness, Knoop Hardness, andScleroscope HardnessF 899 Specification for Wrought Stainless Steels for Surgi-cal InstrumentsF 921 Terminology Relating to Hemostatic Forceps3. Terminol
5、ogy3.1 Definitions applicable to hemostatic forceps shall be inaccordance with Definitions F 921.4. Material4.1 All of the component parts of the instruments shall bemade of martensitic stainless steel of Type 410, 410X, 416,416MOD, 420A, or 420B of Specification F 899.5. Physical Requirements5.1 He
6、at Treatment and Hardness for Component Parts:5.1.1 The component parts of the instruments shall be heattreated under conditions recommended for the material used.Typical heat treating guidelines and hardness values are shownin Specification F 899.5.1.2 The hardness of all opposing parts of the same
7、instrument shall not vary in hardness by more than 4 units onthe Rockwell Hardness C scale (HRC) or equivalent.5.2 PassivationInstruments and instrument componentsshall be passivated after completion of all fabricating andfinishing operations.6. Performance Requirements6.1 Finger RingsInside surface
8、s shall be well roundedand polished and shall comply with the requirements in 7.1.6.2 Jaw Serrations and TeethJaw serrations and teethshall be of the types specified in Definitions F 921. Theserrations and teeth shall be of uniform depth and height andwell defined to provide effective gripping. The
9、serrations andteeth shall interdigitate. The edges of the serrations shall bechamfered.6.3 Box LockThe hemostatic forceps shall be of box lockconstruction, as defined in Definitions F 921. The pin, or otherfastening component, shall be permanently secured. The jointperformance of the box lock shall
10、be smooth, of equalresistance, and non-binding when opening or closing theforceps to an included angle of 90 6 5 (the lock may belubricated).6.4 ClearanceThe maximum clearance between the maleand female members of the forceps in the lock area shall be 0.4mm (0.015 in.). The clearance is the visible
11、gap that existswhen the instrument is viewed from both the front and sideprofile or end view of the instrument (excluding bevel) (seeFig. 1).6.5 RatchetsRatchet and ratchet catch shall securely en-gage at each ratchet position in a smooth and progressivemanner.6.6 Jaw and Ratchet SettingThe jaw tips
12、 shall close andinterdigitate when the first ratchet position is engaged, andthere shall be no visible misalignment of the jaws. The jaws1This specification is under the jurisdiction of ASTM Committee F04 onMedical and Surgical Materials and Devices and is the direct responsibility ofSubcommittee F0
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