← Back to catalogue

Pro Pelvic Splint

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
PRO PELVIC SPLINT FDA UDI
Generic Name
Pelvic fracture binder, reusable FDA UDI
Device Name
PRO PELVIC SPLINT 1 ea - 6 mm Neoprene Band, 1 ea - Black Velcro Straps with Buckle Intended for the emergency management of suspected pelvic fracture(s). FDA UDI
Model / Reference
02 FDA UDI
Description
PRO PELVIC SPLINT 1 ea - 6 mm Neoprene Band, 1 ea - Black Velcro Straps with Buckle Intended for the emergency management of suspected pelvic fracture(s). FDA UDI

Identifiers

Catalog Number
55-110 FDA UDI
Primary DI / UDI-DI
M68955110020 FDA UDI
FDA Product Code
HSQ FDA UDI
GMDN Term
Pelvic fracture binder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5890 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pelvic fracture binder, reusable

Pro Pelvic Splint by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic fracture binder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Safeguard Us Operating, Llc

Sources (1)

  • FDA UDI 75276dc2-8c73-493c-aed0-27b3c3f96c75 35 fields · synced May 31, 2026