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Capiox

FDA UDI

Class I (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
CAPIOX FDA UDI
Generic Name
Medical device service rail clamp FDA UDI
Device Name
Device Holder FDA UDI
Model / Reference
XX*XH032 FDA UDI
Description
Device Holder FDA UDI

Identifiers

Catalog Number
XX*XH032 FDA UDI
Primary DI / UDI-DI
04987350734617 FDA UDI
FDA Product Code
KRI FDA UDI
GMDN Term
Medical device service rail clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Medical device service rail clamp

Capiox by Terumo Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device service rail clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI f4f05fab-53d5-4c8c-b1db-f2c3c5cbdfc2 36 fields · synced Jun 7, 2026