Sontec S-Curve Retractor 207-418

GUDID 00192896120372

Hand-held surgical retractor, reusable

Primary Device ID	00192896120372
NIH Device Record Key	1d44937b-33ff-4581-9997-e24bf6d42a01
Commercial Distribution Status	In Commercial Distribution
Brand Name	Sontec S-Curve Retractor
Version Model Number	207-418
Catalog Number	207-418
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
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	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00192896120372 [Primary]

RETRACTOR

Steralize Prior To Use	true
Device Is Sterile	false

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

[00192896120372]

Dry Heat Sterilization

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