DEVICE: Unite Medical® (00850012035312)

Device Identifier (DI) Information

Unite Medical®
Cryo Pneumatic Shoulder - Universal
In Commercial Distribution
Cyro3670
Unite Medical, LLC
00850012035312
GS1

1
117553945 *Terms of Use
The Unite Medical® Cryo Pneumatic Shoulder orthosis combines pneumatic compression with cold therapy in a universal design. Indicated for post-op application or as an adjuct to a physical therapy regime, the Cryo Pneumatic Shoulder orthosis offers a wide variety of treatment options. Aids in the reduction of swelling, reduced muscle spasms, and pain relief.
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Device Characteristics

Labeling does not contain MRI Safety Information
No
Yes
No
No
Yes
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
37240 Hot/cold therapy pack, reusable
A non-sterile device intended to be applied with or without pressure to the body surface (i.e., non-invasively) to provide heat and/or cold therapy for the skin and/or underlying tissues in the treatment of musculoskeletal pain and discomfort (e.g., from sports injuries or rheumatism). It consists of a compact envelope filled with a thermally-retentive material (e.g., silicate-based gel) that can be heated and/or cooled. It may be shaped/sized to fit a specific anatomy or include a strap; it is not intended to support the neck. This is a reusable device.
Active false
12101 Shoulder immobilizer/orthosis, reusable
A prefabricated (non-customized) non-rigid wearable device designed to support, align, and/or temporarily immobilize the shoulder joint to support the healing of an injury or surgical wound. It will typically consist of straps, buckles, fasteners, or be in the form of a sling. This is a reusable device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
IQQ Joint, Shoulder, External Limb Component
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FDA Premarket Submission

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

Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

76d4d2a9-498a-4b00-a4d3-e375a30af162
June 28, 2024
1
June 20, 2024
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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
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Secondary DI

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Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
No
Yes
No CLOSE

Customer Contact

[?]
833-868-6483
info@unitemedical.net
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