AccessGUDID - DEVICE: NA (10887587015675)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: 04.315.127
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 04315127
Company Name: Synthes GmbH

Primary DI Number: 10887587015675
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 486711679 *Terms of Use

Device Description: REMOVABLE EXTENSION ARM-FLEX 40MM FOR CMF DISTRACTOR

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
47636	Craniofacial bone distractor extension	A partially-implantable device intended to be temporarily used as an extension for an implanted or partially-implanted craniofacial distractor allowing connection to the central adjustment thread of the distractor when its location is made difficult to access due to its surgical positioning. It is used to allow the required rotation of the thread in order to distract (force apart) the two bone surfaces of the mandibular body (the lower jawbone) during the adjustment period. It is typically made of high-grade stainless steel and may be rigid or flexible in design.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
MQN	EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR
PBJ	Cranial Distraction System

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K060138	000
K080153	000
K162594	000
K170818	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ac41ef17-1b16-4983-b846-b23dcfac3997
Public Version Date: April 25, 2022
Public Version Number: 6
DI Record Publish Date: September 14, 2015

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
HIBCC	H980043151270

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

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

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