Trulife 630JD04

by Trulife Inc.

Trulife 630JD04 is a Class I device made by Trulife Inc., listed in FDA GUDID since 31 Dec 2022 (UDI-DI 00645517725529), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00645517725529 UDI-DI	Date31 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00645517725529

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trulife
Generic name: Abdominal binder, reusable
Model / reference: 630JD04

Primary DI / UDI-DI: 00645517725529
FDA product code: NOJ
GMDN term: Abdominal binder, reusable

Device class: Class I
Regulation number: 878.3800
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Abdominal binder, reusable.

Other devices from Trulife Inc.

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Properties

Single use
Over-the-counter
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (10, all answered No)