Oktagon® 82870

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

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

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberE0HM7082870DU00001 UDI-DI	Date15 Sep 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Oktagon®
Generic Name: Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog: 82870

Primary DI / UDI-DI: E0HM7082870DU00001
FDA Product Code: OFY
GMDN Term: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Device Class: Class I
Regulation Number: 872.3980
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Class I
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Class I

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Properties

Prescription Use
Convenience Kit
Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (9)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No