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Cp Fiber

FDA UDI

Class II (US FDA UDI)

by Cp Medical

Identity

Trade Name
CP FIBER FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Model / Reference
CPF-40-18-DA FDA UDI

Identifiers

Catalog Number
CPF-40-18-DA FDA UDI
Primary DI / UDI-DI
10790986004631 FDA UDI
510(k) Number
K041894 FDA UDI
K094028 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyolefin/fluoropolymer suture, multifilament

Cp Fiber by Cp Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, multifilament.

Cleared under the same submission

K041894 also covers:

K094028 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cp Medical

Sources (1)

  • FDA UDI b5e7e6ae-6fd4-4c06-ad19-d791f8569ce2 34 fields · synced May 31, 2026