SEARCH RESULTS FOR: ("hf acquisition co")(39637 results)

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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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ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
0801522X34
In Commercial Distribution

  • B5820801522X340 ()
0801522X34

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
080152234
In Commercial Distribution

  • B5820801522340 ()
080152234

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
080152214
In Commercial Distribution

  • B5820801522140 ()
080152214

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
080152212
In Commercial Distribution

  • B5820801522120 ()
080152212

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
080151312
In Commercial Distribution

  • B5820801513120 ()
080151312

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
0801508
In Commercial Distribution

  • B58208015080 ()
0801508

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
0801506
In Commercial Distribution

  • B58208015060 ()
0801506

  • Bone lever/elevator, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
0801501
In Commercial Distribution

  • B58208015010 ()
0801501

  • Bone lever/elevator, reusable
CURETTE
GEORGE TIEMANN & CO.
08014353
In Commercial Distribution

  • B582080143530 ()
08014353

  • Dermal curette, single-use
CURETTE
GEORGE TIEMANN & CO.
08014156
In Commercial Distribution

  • B582080141560 ()
08014156

  • Dermal curette, single-use
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