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Deknatel

FDA UDI

Class U (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
DEKNATEL FDA UDI
Generic Name
Bone wax, natural FDA UDI
Device Name
Bone Wax Contents: One (1) Bars 2.5 Grams FDA UDI
Model / Reference
IPN029172 FDA UDI
Description
Bone Wax Contents: One (1) Bars 2.5 Grams FDA UDI

Identifiers

Catalog Number
BW-102 FDA UDI
Primary DI / UDI-DI
14026704635655 FDA UDI
510(k) Number
K050292 FDA UDI
FDA Product Code
MTJ FDA UDI
GMDN Term
Bone wax, natural FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Bone wax, natural

Deknatel by Teleflex Incorporated — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone wax, natural.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06df0322-1f45-4240-a77f-38f7ed2468f2 36 fields · synced May 30, 2026