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Chronoceptor™

FDA UDI

Class I (US FDA UDI)

by Merete GmbH

Identity

Trade Name
Chronoceptor™ FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
Chronoceptor for 2.0 and 2.5 Mecron Screws with length gauge 8-50 AO-connector color-coated white and magenta sterile FDA UDI
Model / Reference
CH15100S FDA UDI
Description
Chronoceptor for 2.0 and 2.5 Mecron Screws with length gauge 8-50 AO-connector color-coated white and magenta sterile FDA UDI

Identifiers

Primary DI / UDI-DI
04048266181183 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluted surgical drill bit, single-use

Chronoceptor™ by Merete GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merete GmbH

Sources (1)

  • FDA UDI d4b76476-5149-4789-a0f2-9141346b464c 34 fields · synced May 30, 2026