214639

GUDID 10886705004201

STABILIZATION OBTURATOR Introducing device used w/Mitek drill guides

Medos International Sàrl

Surgical drill guide obturator

Primary Device ID	10886705004201
NIH Device Record Key	57dba15a-049c-4379-83ce-e71e6670d611
Commercial Distribution Status	In Commercial Distribution
Version Model Number	214639
Catalog Number	214639
Company DUNS	482661753
Company Name	Medos International Sàrl
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	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx
Phone	+1(800)255-2500
Email	xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705004201 [Primary]

FDA Product Code

LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

[10886705004201]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2024-03-08
Device Publish Date	2015-09-01

Devices Manufactured by Medos International Sàrl

10705034219318 - EXPEDIUM	2026-02-09 EXPEDIUM ANTERIOR SPINE SYSTEM SINGLE-HOLE IMPACTOR, MODULAR
10705034219325 - EXPEDIUM	2026-02-09 EXPEDIUM ANTERIOR SPINE SYSTEM DUAL HOLE STAPLE IMPACTOR
10705034219332 - EXPEDIUM	2026-02-09 EXPEDIUM ANTERIOR SPINE SYSTEM FINISHING IMPACTOR, MODULAR
10705034467368 - EXPEDIUM	2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER, CAP
10705034467375 - EXPEDIUM	2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER, BODY
10705034467382 - EXPEDIUM	2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER ASSEMBLY
10705034647074 - TELIGEN	2025-12-18 TELIGEN Dilator Large
10705034647081 - TELIGEN	2025-12-18 TELIGEN Dilator Medium

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