Spencer Wells, Artery Forcep Straight, 150mm Length

GUDID 05056405517150

PLATTS & NISBETT LIMITED

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 ID05056405517150
NIH Device Record Keyb4d50595-569b-4ef9-90b9-137d443b6ac4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSpencer Wells, Artery Forcep Straight, 150mm Length
Version Model NumberPN1594
Company DUNS290712512
Company NamePLATTS & NISBETT LIMITED
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
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 Identifiers

Device Issuing AgencyDevice ID
GS105056405517150 [Primary]

FDA Product Code

HTDForceps

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


[05056405517150]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-27
Device Publish Date2023-09-19

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