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NS10675 Safety Foam

FDA UDI

Class I (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
NS10675 Safety Foam FDA UDI
Generic Name
Surgical instrument interim-placement holder, single-use FDA UDI
Device Name
NS10675 Safety Foam FDA UDI
Model / Reference
NS10675 FDA UDI
Description
NS10675 Safety Foam FDA UDI

Identifiers

Catalog Number
NS10675 FDA UDI
Primary DI / UDI-DI
00787551012002 FDA UDI
FDA Product Code
GAB FDA UDI
GMDN Term
Surgical instrument interim-placement holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument interim-placement holder, single-use

NS10675 Safety Foam by Xodus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xodus Medical, Inc.

Sources (1)

  • FDA UDI ffb4e80b-7d9a-4745-945f-4ffb8a1222dd 35 fields · synced Jun 6, 2026