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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RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801869S
In Commercial Distribution

  • B582801869S0 ()
801869S

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801869L
In Commercial Distribution

  • B582801869L0 ()
801869L

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801867
In Commercial Distribution

  • B5828018670 ()
801867

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801866
In Commercial Distribution

  • B5828018660 ()
801866

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801865
In Commercial Distribution

  • B5828018650 ()
801865

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801861
In Commercial Distribution

  • B5828018610 ()
801861

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801860
In Commercial Distribution

  • B5828018600 ()
801860

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
801856
In Commercial Distribution

  • B5828018560 ()
801856

  • Hand-held surgical retractor, reusable
CURETTE
GEORGE TIEMANN & CO.
80143530
In Commercial Distribution

  • B582801435300 ()
80143530

  • Dermal curette, single-use
CURETTE
GEORGE TIEMANN & CO.
80143520
In Commercial Distribution

  • B582801435200 ()
80143520

  • Dermal curette, single-use
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