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Cryomatic Console

FDA UDI

Class II (US FDA UDI)

by Keeler Limited

Identity

Trade Name
Cryomatic Console FDA UDI
Generic Name
Ophthalmic cryosurgical system, electronic FDA UDI
Model / Reference
2509-P-1000 FDA UDI

Identifiers

Primary DI / UDI-DI
05055272707633 FDA UDI
FDA Product Code
HRN FDA UDI
GMDN Term
Ophthalmic cryosurgical system, electronic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4170 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

No

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: Ophthalmic cryosurgical system, electronic

Cryomatic Console by Keeler Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic cryosurgical system, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keeler Limited

Sources (1)

  • FDA UDI b1342be3-e11a-448a-acea-489d1ab9dbfa 32 fields · synced May 30, 2026