SEARCH RESULTS FOR: 制作AT(525736 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 - 00885556604298

REFURB DUCKLING STRAIGHT
Smith & Nephew, Inc.
012044D
Not in Commercial Distribution

  • 00885556604298 ()
012044D

  • Meniscus knife

N/A - 00885556600221

O*SOD BSKT PCH CAP RELEASE FRCP UPBTR
Smith & Nephew, Inc.
3134131
Not in Commercial Distribution

  • 00885556600221 ()
3134131

  • Meniscus knife

N/A - 00885556600122

SOD PUNCH SCOOP STRT 1.0MM
Smith & Nephew, Inc.
3134076
Not in Commercial Distribution

  • 00885556600122 ()
3134076

  • Meniscus knife

N/A - 00885556504635

REFURB MICROPUNCH TEARDROP LEFT
Smith & Nephew, Inc.
7207602D
In Commercial Distribution

  • 00885556504635 ()
7207602D

  • Meniscus knife

N/A - 00885556504628

REFURB MICROGRASPER UPBITER
Smith & Nephew, Inc.
7207599D
Not in Commercial Distribution

  • 00885556504628 ()
7207599D

  • Meniscus knife

N/A - 00885556504574

REFURB PCH OVAL STR
Smith & Nephew, Inc.
7207201D
Not in Commercial Distribution

  • 00885556504574 ()
7207201D

  • Meniscus knife

N/A - 00885556504567

REFURB.PCH OVAL UPBTR 15D
Smith & Nephew, Inc.
7207200D
Not in Commercial Distribution

  • 00885556504567 ()
7207200D

  • Meniscus knife

N/A - 00885556658079

MTO PNCH.BSKT.NRWLN.UPBTR.CRVD RT.
Smith & Nephew, Inc.
3134042
Not in Commercial Distribution

  • 00885556658079 ()
3134042

  • Meniscus knife

FEMORAL HEAD DISARTICULATOR KNIFE - 00192896090040

FEMORAL HEAD DISARTICULATOR KNIFE SMALL SIZE CURVED BLADE
SONTEC INSTRUMENTS, INC.
1103-211
In Commercial Distribution

  • 00192896090040 ()

  • Length: 5.5 Inch
1103-211

  • Meniscus knife

N/A - 03596010507341

REFURB ROTARY BASKET PUNCH 90 DEG
Smith & Nephew, Inc.
010900D
Not in Commercial Distribution

  • 03596010507341 ()
010900D

  • Meniscus knife
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