REFLEX ZERO-PROFILE 48513011

GUDID 07613327270969

PLATE BENDER

Stryker Corporation

Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable

Primary Device ID	07613327270969
NIH Device Record Key	458d257b-0db5-45e8-a450-dc296a71a595
Commercial Distribution Discontinuation	2024-07-04
Commercial Distribution Status	In Commercial Distribution
Brand Name	REFLEX ZERO-PROFILE
Version Model Number	48513011
Catalog Number	48513011
Company DUNS	149183167
Company Name	Stryker Corporation
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327270969 [Primary]

FDA Product Code

LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT