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Codman

FDA UDI

Class II (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN FDA UDI
Generic Name
Neurosurgical sponge FDA UDI
Device Name
CODMAN Bulk Surgical Patties X-Ray Detectable 1/2 Inch x 1 Inch (1.27cm x 2.54cm) FDA UDI
Model / Reference
24-5406 FDA UDI
Description
CODMAN Bulk Surgical Patties X-Ray Detectable 1/2 Inch x 1 Inch (1.27cm x 2.54cm) FDA UDI

Identifiers

Catalog Number
245406 FDA UDI
Primary DI / UDI-DI
20886704004155 FDA UDI
510(k) Number
K880402 FDA UDI
FDA Product Code
HBA FDA UDI
GMDN Term
Neurosurgical sponge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4700 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Codman by Cerenovus, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K880402 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cerenovus, Inc.

Sources (1)

  • FDA UDI 010fa347-41e5-4f02-bcba-d74072eb8400 37 fields · synced Jun 1, 2026