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Typenex Wound Drainage

FDA UDI

Class I (US FDA UDI)

by Typenex Medical, LLC

Identity

Trade Name
Typenex Wound Drainage FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
10 mm Flat Fluted, 3/4 size with Trocar FDA UDI
Model / Reference
WD0602PT FDA UDI
Description
10 mm Flat Fluted, 3/4 size with Trocar FDA UDI

Identifiers

Primary DI / UDI-DI
00812269030717 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Typenex Wound Drainage by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5fa02bb-66dc-40ad-a8ac-505714d6f246 33 fields · synced May 31, 2026