ELITE MEDICAL INSTRUMENTATION EMI-BF122R SSPONGE STICK

GUDID G569EMIBF122R0

Sponge Stick, Foerster, Serrated, Straight, 9 1/2"

ELITE MEDICAL INSTRUMENTATION

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDG569EMIBF122R0
NIH Device Record Keyb5391e7d-38c8-4809-8896-e8e2e26cde57
Commercial Distribution StatusIn Commercial Distribution
Brand NameELITE MEDICAL INSTRUMENTATION
Version Model NumberEMI-BF122R
Catalog NumberEMI-BF122R SSPONGE STICK
Company DUNS116733674
Company NameELITE MEDICAL INSTRUMENTATION
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCG569EMIBF122R0 [Primary]

FDA Product Code

HTDForceps

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


[G569EMIBF122R0]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-29
Device Publish Date2024-03-21

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G569EMIKTS3170Love-Gruenwald Rongeur, Up Bite, 3x10mm, 180mm
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G569EMIKTS3100Kerrison, 40 Down, 1mm, Thin Footplate, 180mm
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G569EMIKTS3070Kerrison, 90 Down, 1mm, Thin Footplate, 180mm
G569EMIKTS3060Kerrison, 90 Up, 3mm, Thin Footplate, 180mm
G569EMIKTS3050Kerrison, 90 Up, 2mm, Thin Footplate, 180mm
G569EMIKTS3040Kerrison, 90 Up, 1mm, Thin Footplate, 180mm
G569EMIKTS3030Kerrison, 40 Up, 3mm, Thin Footplate, 180mm
G569EMIKTS3020Kerrison, 40 Up, 2mm, Thin Footplate, 180mm
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