← Back to catalogue

9° and 15° Distractor Tray

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ASY-00420

by Integrity Implants Inc.

Identity

Trade Name
9° and 15° Distractor Tray EUDAMED
N/A FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
FlareHawk Trays EUDAMED
9 and 15 Degree Distractor Tray FDA UDI
Model / Reference
ASY-00420 EUDAMEDFDA UDI
Description
9 and 15 Degree Distractor Tray FDA UDI

Identifiers

Catalog Number
ASY-00420 FDA UDI
Primary DI / UDI-DI
00810004728332 EUDAMEDFDA UDI
Basic UDI-DI
0081000472FHTRAYSUH EUDAMED
Direct Marketing DI
00810004728332 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

9° and 15° Distractor Tray by Integrity Implants Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000009805
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 016ba704-7914-46bd-9eb9-8b789df5dccf 61 fields · synced Jul 12, 2026
  • FDA UDI 70673c2a-97a6-4374-aa86-7252aa355783 35 fields · synced May 30, 2026