0785-045-016

GUDID 07613327261301

Restraint Strap

STRYKER CORPORATION

Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable Limb/torso/head restraint, reusable
Primary Device ID07613327261301
NIH Device Record Key2c6dd5f1-9c6c-4e8c-8b07-abd895a48ca6
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0785-045-016
Catalog Number0785-045-016
Company DUNS078470558
Company NameSTRYKER CORPORATION
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 Batchfalse
Serial Numbertrue
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
GS107613327261301 [Primary]

FDA Product Code

FPOSTRETCHER, WHEELED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-18
Device Publish Date2020-09-10

Devices Manufactured by STRYKER CORPORATION

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07613327623796 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HIP
07613327623833 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
07613327634686 - Iconix2024-03-12 Iconix DC Guide for 1.4mm anchor
07613327634693 - Iconix2024-03-12
07613327616675 - SPY2024-03-06
07613327616682 - SPY2024-03-06

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