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Cen-Step™

FDA UDI

Class I (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Cen-Step™ FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Model / Reference
00884450406953 FDA UDI

Identifiers

Catalog Number
CSC-5F-7S FDA UDI
Primary DI / UDI-DI
00884450406953 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Closed-wound drain, non-bioabsorbable

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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 d21802d2-a9e1-411d-adb9-e97efdba3b61 34 fields · synced Jul 19, 2026