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CereLink™

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
CereLink™ FDA UDI
Generic Name
Intracranial/compartmental-pressure monitor calibrator/cable FDA UDI
Device Name
CereLink™ ICP Extension Cable FDA UDI
Model / Reference
826845 FDA UDI
Description
CereLink™ ICP Extension Cable FDA UDI

Identifiers

Catalog Number
82-6845 FDA UDI
Primary DI / UDI-DI
10381780520665 FDA UDI
FDA Product Code
GWM FDA UDI
GMDN Term
Intracranial/compartmental-pressure monitor calibrator/cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1620 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Intracranial/compartmental-pressure monitor calibrator/cable

CereLink™ by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracranial/compartmental-pressure monitor calibrator/cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 824df48a-9347-404e-8467-a9f5a052aa14 36 fields · synced Jun 9, 2026