C37 医疗设备通用要求 标准查询与下载



共找到 713 条与 医疗设备通用要求 相关的标准,共 48

Requirements for marking of in vitro diagnostic instruments.

ICS
11.100.10
CCS
C37
发布
1997-02-01
实施
1997-02-05

MIL-STD-600006, dated 13 April 1992, and any subsequent revisions or change notices are inactive for new design and shall no longer be used for new designs.

VECTOR PRODUCT FORMAT [Superseded By: DOD MIL-STD-2407 ADMIN NOTICE 2, DOD MIL-STD-2407 CHG NOTICE 1, DOD MIL-STD-2407]

ICS
CCS
C37
发布
1997
实施

Настоящий стандарт распространяется на безопасность МЕДИЦИНСКИХ ЭЛЕКТРИЧЕСКИХ ИЗДЕЛИЙ. Так как настоящий стандарт относится в основном

Medical electrical equipment. Part 2. Particular requirements for safety of transport incubators

ICS
11.040.10
CCS
C37
发布
1997
实施
1998-01-01

This Commercial Item Description covers a portabie,battery operated, rechargeable, volumetric intravenous infusion

PUMP, INTRAVENOUS INFUSION

ICS
CCS
C37
发布
1996-08-16
实施

In vitro diagnostic systems. Transport packages for medical and biological specimens. Requirements, tests.

ICS
11.100.10;55.040
CCS
C37
发布
1996-06-01
实施
1996-06-20

In vitro diagnostic systems. Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices.

ICS
11.100.10
CCS
C37
发布
1996-01-01
实施
1996-01-05

Настоящий стандарт распространяется на безопасность МЕДИЦИНСКИХ ЭЛЕКТРИЧЕСКИХ ИЗДЕЛИЙ. Так как настоящий стандарт относится в основном

Medical electrical equipment. Part 2. Particular requirements for safety of baby incubators

ICS
11.040.10
CCS
C37
发布
1996
实施
1998-01-01

本标准规定了电热蒸馏水器的产品分类、技术要求、试验方法、检验规则以及标志、包装、运输、贮存等要求。 本标准适用于电热蒸馏水器,该产品供医疗卫生单位制取蒸馏水用。

Electrical heat water still

ICS
11.080.10
CCS
C37
发布
1995-11-14
实施
1996-05-01

This military handbook is approved for use by all Departments and Agencies of the Department of Defense.

DEPARTMENT OF DEFENSE APPLICATION OF MIL-PRF-28001 USING STANDARD GENERALIZED MARKUP LANGUAGE (SGML)

ICS
CCS
C37
发布
1995-06-30
实施

This specification covers National Stock Number (NSN) 6515-00-616-5052 , Laryngoscope, Infant-Child-Adult, MacIntosh;and in additon, the following components when procured as individual items of supply (see below) with their respective item identificati

LARYNGOSCOPE SET, MACINTOSH

ICS
CCS
C37
发布
1995-06-30
实施

The lens shall consist of three parts: a molded plastic cup-shaped lens with nipple on top for tubing connection to allow entrance of fluid, a tubing and adaptor for universal fit to IV systems. It shall be a sterile, one time use disposable type, indivi

LENS, SCLERAL, OCULAR LAVAGE

ICS
CCS
C37
发布
1995-02-21
实施

The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Federal Specification DDD-C-800A, which is cancelled.

CURTAIN, BEDSIDE SCREEN

ICS
CCS
C37
发布
1995-01-20
实施

IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).

ICS
11.100
CCS
C37
发布
1995-01
实施
1994-12-05

IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR USER MANUALS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR HOME USE. (EUROPEAN STANDARD EN 592).

ICS
11.100
CCS
C37
发布
1995-01
实施
1994-12-05

Настоящий стандарт распространяется на безопасность МЕДИЦИНСКИХ ЭЛЕКТРИЧЕСКИХ ИЗДЕЛИЙ. Так как настоящий стандарт относится в основном

Medical electrical equipment. Part 2. Particular requirements for the safety of transcutaneous partial pressure monitoring equipment

ICS
11.040.55
CCS
C37
发布
1995
实施
1997-01-01

This Commercial Item Description covers cutaneous biopsy punches of Keyes design suitable for cutting biopsy of skin lesions.

PUNCH, CUTANEOUS BIOPSY, KEYES

ICS
49.050
CCS
C37
发布
1994-09-30
实施

Curettes shall be of the Billeau design with a flexible, oval shaped, medium size loop that is securely attached to the shank. The junction shall not have voids or crevices.shall be securely assembled.Shanks and handles manufactured from two pieces

CURETTE, EAR, BILLEAU

ICS
CCS
C37
发布
1994-09-30
实施

The General Services Administration has authorized the use of this Commercial Item Description.

SUTURE, ABSORBABLE, SURGICAL, GUT

ICS
CCS
C37
发布
1994-09-09
实施

Shall be black, braided, unarmed, surgical silk sutures. The size and length of every suture covered by this document shall be as specified below. Sutures shall comply with the latest United States Pharmacopeia (USP) - requirements for "Class I Nonabsorb

SUTURE NONABSORBABLE SURGICAL, SILK

ICS
CCS
C37
发布
1994-09-09
实施

Shall be black, monofilament, nylon surgical sutures. The size , length, and arming of every suture covered by this document shall be as specified below. The type of needle(s) specified below shall be attached to the suture. The shape and length of the n

SUTURE, NONABSORBABLE, SURGICAL, NYLON

ICS
CCS
C37
发布
1994-09-09
实施



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