← Back to catalogue

CryoDose

FDA UDI

Class II (US FDA UDI)

by Nuance Medical, Llc

Identity

Trade Name
CryoDose FDA UDI
Generic Name
General cryosurgical system, cryogen gas, mechanical FDA UDI
Device Name
CryoDose 162 mL (175 g) Reusable Treatment Kit (80 Buds) FDA UDI
Model / Reference
1103 FDA UDI
Description
CryoDose 162 mL (175 g) Reusable Treatment Kit (80 Buds) FDA UDI

Identifiers

Catalog Number
1103 FDA UDI
Primary DI / UDI-DI
00856331006033 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
General cryosurgical system, cryogen gas, mechanical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 162 Milliliter FDA UDI

Category: General cryosurgical system, cryogen gas, mechanical

CryoDose by Nuance Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General cryosurgical system, cryogen gas, mechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nuance Medical, Llc

Sources (1)

  • FDA UDI cf1b2d4c-4818-4eec-a76c-2967c16fb5f0 37 fields · synced May 30, 2026