Perfix™ MIS

GUDID 08800015947596

U&I CORPORATION

Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable

Primary Device ID	08800015947596
NIH Device Record Key	2f8ede93-2052-4477-8785-5f34fb4438d0
Commercial Distribution Status	In Commercial Distribution
Brand Name	Perfix™ MIS
Version Model Number	SS0080
Company DUNS	688811082
Company Name	U&I 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	true
Manufacturing Date	false
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

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool dry place.

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800015947596 [Primary]

FDA Product Code

FZX	Guide, surgical, instrument