Comply™ 1250

Comply™ 1250 is a Class II device made by 3M Company, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 30707387230259), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number30707387230259 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 30707387230259

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Comply™
Generic name: Chemical/physical sterilization process indicator
Model / Ref / Catalog: 1250

Primary DI / UDI-DI: 30707387230259
FDA product code: JOJ
GMDN term: Chemical/physical sterilization process indicator

Device class: Class II
Regulation number: 880.2800
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Premarket exempt
Lot / batch number
Expiration date

Other properties (11, all answered No)