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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
0801306
In Commercial Distribution

  • B58208013060 ()
0801306

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
0801261
In Commercial Distribution

  • B58208012610 ()
0801261

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
0801251
In Commercial Distribution

  • B58208012510 ()
0801251

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
801225
In Commercial Distribution

  • B58208012250 ()
801225

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
0801221
In Commercial Distribution

  • B58208012210 ()
0801221

  • Suturing unit, reusable
IMPACTOR
GEORGE TIEMANN & CO.
0801216
In Commercial Distribution

  • B58208012160 ()
0801216

  • Orthopaedic implant impactor, reusable
IMPACTOR
GEORGE TIEMANN & CO.
0801213
In Commercial Distribution

  • B58208012130 ()
0801213

  • Orthopaedic implant impactor, reusable
IMPACTOR
GEORGE TIEMANN & CO.
0801212
In Commercial Distribution

  • B58208012120 ()
0801212

  • Orthopaedic implant impactor, reusable
IMPACTOR
GEORGE TIEMANN & CO.
0801205
In Commercial Distribution

  • B58208012050 ()
0801205

  • Orthopaedic implant impactor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801202
In Commercial Distribution

  • B58208012020 ()
801202

  • Hand-held surgical retractor, reusable
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