AccessGUDID - DEVICE: NA (10886982240071)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: 530.660
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 530660
Company Name: Synthes GmbH

Primary DI Number: 10886982240071
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 486711679 *Terms of Use

Device Description: INSERTION SHIELD FOR BATTERY POWER LINE II

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:	No
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?
47867	Surgical power tool battery-exchange sterility cover	A cover that functions as a physical barrier between a battery and the sterile battery-powered surgical power tool (e.g., a drill or saw) in which the non-sterile battery is being placed/exchanged prior to or during a surgical procedure. It is typically made from high-grade stainless steel and/or synthetic material and is designed as a flange that fits into/around the slot where the battery is housed (typically in the handle of the power tool). This ensures that no contact is made between the sterile power tool and the person holding it inside the sterile operation field and the non-sterile battery and person loading the battery from outside the sterile field. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MOQ	BATTERY, REPLACEMENT, RECHARGEABLE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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: e0d8d211-d505-4fd6-a09f-fe277b60f899
Public Version Date: April 18, 2022
Public Version Number: 3
DI Record Publish Date: May 22, 2017

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	H6795306600

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: Yes
DM DI Number: 07611819491816
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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