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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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LOCKHART-MUMMERY Fistula Probe, straight, 6 1/2" (165 mm), Fig. 1
Aesculap AG
BN021R
In Commercial Distribution

  • 04038653029204 ()
BN021R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
NELATON Director, curved, 6 1/4" (160 mm)
Aesculap AG
BN012R
In Commercial Distribution

  • 04038653029198 ()
BN012R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
DOYEN Director, curved, 5 3/4" (145 mm)
Aesculap AG
BN010R
In Commercial Distribution

  • 04038653029181 ()
BN010R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
Director, straight, 6 1/4" (160 mm)
Aesculap AG
BN006R
In Commercial Distribution

  • 04038653029174 ()
BN006R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
Director, straight, 5 3/4" (145 mm)
Aesculap AG
BN004R
In Commercial Distribution

  • 04038653029167 ()
BN004R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
Director, straight, 5 1/8" (130 mm)
Aesculap AG
BN003R
In Commercial Distribution

  • 04038653029150 ()
BN003R

  • Abdominal/ENT/orthopaedic surgical probe, reusable
Sterile needle guide
CIVCO MEDICAL INSTRUMENTS CO., INC.
610-1187, 610-1198
In Commercial Distribution

  • 00841436102315 ()
  • 00841436102308 ()
  • 10841436102305 ()

  • Width: 3 Inch
  • Length: 2.5 Inch
610-1187, 610-1198

  • Needle guide, single-use
NIB FOR ECKHOFF PEN ONLY
Aesculap AG
BA705
Not in Commercial Distribution

  • 04038653338283 ()
  • 04038653019694 ()
BA705

  • Skin marking pen, reusable
STRAINER F/TISSUE F/SINGLE USE PLASTIC
Aesculap AG
GF722
Not in Commercial Distribution

  • 04038653005956 ()
GF722

  • Suction/irrigation tubing, single-use
BDS RONG R2 BLUMNTHL 6" 300 PREM
NORDENT MANUFACTURING INC
R2/BH
In Commercial Distribution

  • 00840018604193 ()


  • Dental rongeur
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