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Trulife

FDA UDI

Class I (US FDA UDI)

by Trulife, Inc.

Identity

Trade Name
Trulife FDA UDI
Generic Name
Thoracic spine orthosis FDA UDI
Device Name
RIGID BACK SUPPORT PANEL FOR 7210 LOW TEMP INSERT FDA UDI
Model / Reference
PT740 FDA UDI
Description
RIGID BACK SUPPORT PANEL FOR 7210 LOW TEMP INSERT FDA UDI

Identifiers

Primary DI / UDI-DI
00645517585567 FDA UDI
FDA Product Code
ISR FDA UDI
GMDN Term
Thoracic spine orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thoracic spine orthosis

Trulife by Trulife, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thoracic spine orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trulife, Inc.

Sources (1)

  • FDA UDI a26354e6-f101-4507-ba69-e6e7052ae2b0 33 fields · synced Jun 4, 2026