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Axiom® CWV

FDA UDI

Class I (US FDA UDI)

by Axiom Medical, Incorporated

Identity

Trade Name
Axiom® CWV FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
Closed Wound Drain, Flat, Silicone, With Trocar FDA UDI
Model / Reference
803631 FDA UDI
Description
Closed Wound Drain, Flat, Silicone, With Trocar FDA UDI

Identifiers

Primary DI / UDI-DI
M6658036310 FDA UDI
510(k) Number
K965146 FDA UDI
FDA Product Code
GBX 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

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: Closed-wound drain, non-bioabsorbable

Axiom® CWV by Axiom Medical, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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 ddffb7a6-5684-48dc-86a6-c76c30673c21 36 fields · synced May 29, 2026