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Cryo 7

FDA UDI

Class II (US FDA UDI)

by Zimmer MedizinSysteme GmbH

Identity

Trade Name
Cryo 7 FDA UDI
Generic Name
Localized cutaneous/musculoskeletal cryotherapy unit FDA UDI
Model / Reference
7375 FDA UDI

Identifiers

Catalog Number
7375 FDA UDI
Primary DI / UDI-DI
04053815087229 FDA UDI
510(k) Number
K220020 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Localized cutaneous/musculoskeletal cryotherapy unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Localized cutaneous/musculoskeletal cryotherapy unit

Cryo 7 by Zimmer MedizinSysteme GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Localized cutaneous/musculoskeletal cryotherapy unit.

Cleared under the same submission

K220020 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer MedizinSysteme GmbH

Sources (1)

  • FDA UDI b2039933-a9ff-4350-9b0d-a74b215495e2 35 fields · synced Jun 8, 2026