AccessGUDID - DEVICE: UNIMAX (00852647007580)

GUDID

Device Identifier (DI) Information

Brand Name: UNIMAX
Version or Model: 122-18B
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 122-18B
Company Name: PARAMOUNT SURGICALS, INC.

Primary DI Number: 00852647007580
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 015483156 *Terms of Use

Device Description: SQUARE BOLT EXTENDED B TYPE

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?
67309	Bone-screw internal spinal fixation system sterilization container/implant set	A collection of non-sterile, implantable components of a bone-screw internal spinal fixation system (e.g., rods, screws, connectors, hooks) supplied within a reusable sterilization container (i.e., all under the same product code) to be sterilized before they are implanted as part of an internal spinal fixation procedure. The set provides the surgeon with a selection of implants (e.g., different sizes) during surgery, whereby unused implants maybe resterilised for subsequent implantation in another patient. This is a reusable device which includes single-use implants.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
MNH	Orthosis, Spondylolisthesis Spinal Fixation
MNI	Orthosis, Spinal Pedicle Fixation

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K014302	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: 44fff194-7671-44c9-b6b6-1d043a24ef88
Public Version Date: July 02, 2025
Public Version Number: 5
DI Record Publish Date: November 01, 2016

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

Customer Contact

[?]

Phone: 956-541-1220
Email: param@paramountsurgicals.com

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