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Demetech PTFE

FDA UDI

Class II (US FDA UDI)

by DemeTECH Corp

Identity

Trade Name
Demetech PTFE FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Device Name
Synthetic (Polytetrafluoroethylene), Non Absorbable Suture FDA UDI
Model / Reference
TE255013G0P FDA UDI
Description
Synthetic (Polytetrafluoroethylene), Non Absorbable Suture FDA UDI

Identifiers

Primary DI / UDI-DI
10652927671466 FDA UDI
510(k) Number
K181578 FDA UDI
FDA Product Code
NBY FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5035 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyolefin/fluoropolymer suture, monofilament

Demetech PTFE by DemeTECH Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DemeTECH Corp

Sources (1)

  • FDA UDI 54d8a148-c98d-4499-8b19-b6d0ebd892f0 36 fields · synced May 31, 2026