AccessGUDID - DEVICE: Stephens Instruments (00810799031495)

GUDID

Device Identifier (DI) Information

Brand Name: Stephens Instruments
Version or Model: S3-1000
Commercial Distribution Status: In Commercial Distribution
Catalog Number: S3-1000
Company Name: KRISHNA IMPORTS INC

Primary DI Number: 00810799031495
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 081853285 *Terms of Use

Device Description: Castroviejo Blade Breaker, With Lock

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):	No
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?
44959	Razor blade breaker/holder	A surgical instrument specially designed to be used to break, breakable razor blades into shards of extremely sharp segments. Once this is done the instrument can then be used as a safety holder for the segment of broken razor blade, acting as a handle, whilst the surgeon uses it like a scalpel to cut tissue. When the operation is completed the segment of blade is disposed of. Some physicians prefer this method which guarantees the sharpness of the cutting edge. This device is made of high quality stainless-steel alloy and is designed like a short-nosed plier with a locking device to lock the blade segment securely in place. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HXK	HOLDER, NEEDLE; ORTHOPEDIC

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
Special Storage Condition, Specify: Room Temperature

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 3a9f6444-5a6a-4987-a847-c9ec382dae09
Public Version Date: September 30, 2020
Public Version Number: 1
DI Record Publish Date: September 22, 2020

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
No Secondary DIs found

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: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(859)259-4925
Email: info@stephensinst.com

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