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CrOC

FDA UDI

Class II (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
CrOC FDA UDI
Generic Name
Emergency junctional haemorrhage compression set FDA UDI
Device Name
The CRoC is indicated for use in the battlefield to control difficult bleeds in the inguinal and axilla areas. The CRoC is also indicated for use in the battlefield as a last resort for life threatening bleeds of the carotid artery. The CRoC should be applied by a trained medical provider. FDA UDI
Model / Reference
05 FDA UDI
Description
The CRoC is indicated for use in the battlefield to control difficult bleeds in the inguinal and axilla areas. The CRoC is also indicated for use in the battlefield as a last resort for life threatening bleeds of the carotid artery. The CRoC should be applied by a trained medical provider. FDA UDI

Identifiers

Catalog Number
31-200 FDA UDI
Primary DI / UDI-DI
M68931200050 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Emergency junctional haemorrhage compression set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

Yes

FDA UDI

CrOC by Safeguard Us Operating, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Safeguard Us Operating, Llc

Sources (1)

  • FDA UDI b78bd7fc-6d0c-48d6-b921-0df08710a68c 35 fields · synced Jun 1, 2026