SEARCH RESULTS FOR: 得克萨斯A(601548 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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N/A - B5820801590

RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80159
In Commercial Distribution

  • B5820801590 ()
80159

  • Hand-held surgical retractor, reusable

N/A - B5820801580

RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80158
In Commercial Distribution

  • B5820801580 ()
80158

  • Hand-held surgical retractor, reusable

N/A - B5820801570

RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80157
In Commercial Distribution

  • B5820801570 ()
80157

  • Hand-held surgical retractor, reusable

N/A - B5820801550

RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80155
In Commercial Distribution

  • B5820801550 ()
80155

  • Hand-held surgical retractor, reusable

N/A - B5820801530

RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80153
In Commercial Distribution

  • B5820801530 ()
80153

  • Hand-held surgical retractor, reusable

N/A - B5820801522X340

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

  • B5820801522X340 ()
0801522X34

  • Bone lever/elevator, reusable

N/A - B5820801522340

ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
080152234
In Commercial Distribution

  • B5820801522340 ()
080152234

  • Bone lever/elevator, reusable

N/A - B5820801415300

CURETTE
GEORGE TIEMANN & CO.
080141530
In Commercial Distribution

  • B5820801415300 ()
080141530

  • Dermal curette, single-use

N/A - B582080141520

CURETTE
GEORGE TIEMANN & CO.
08014152
In Commercial Distribution

  • B582080141520 ()
08014152

  • Dermal curette, single-use

N/A - B582080141500

CURETTE
GEORGE TIEMANN & CO.
08014150
In Commercial Distribution

  • B582080141500 ()
08014150

  • Dermal curette, single-use
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