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Aa Instrument Case Outer

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 30-036-400Ref 30-037-400Ref 25-053-005

by Symmetry Medical Manufacturing, Inc.

Identity

Trade Name
Femoral Tray FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
AA INSTRUMENT CASE OUTER EUDAMED
Femoral Tray FDA UDI
Model / Reference
30-036-400 EUDAMED
30-037-400 EUDAMEDFDA UDI
25-053-005 EUDAMED
Description
Femoral Tray FDA UDI

Identifiers

Catalog Number
2709-01-000; 30-037-400-1500 FDA UDI
Primary DI / UDI-DI
00847538019209 EUDAMED
00847538019179 EUDAMEDFDA UDI
00847538010817 EUDAMED
Basic UDI-DI
08475380137302K EUDAMED
Direct Marketing DI
00847538019209 EUDAMED
00847538019179 EUDAMED
00847538010817 EUDAMED
FDA Product Code
KCT FDA UDI
EMDN Code
L0919 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Market of Registration
Ireland EUDAMED
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Aa Instrument Case Outer by Symmetry Medical Manufacturing, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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-000025394
Authorised Representative
SYMMETRY MEDICAL POLYVAC FR-AR-000003187

Sources (4)

  • EUDAMED acde3be5-5f72-487e-89b2-e9befb0ccc52 61 fields · synced Oct 6, 2026
  • EUDAMED da03f598-22e1-43bc-8f66-a9c2681b9289 61 fields · synced May 18, 2026
  • EUDAMED 61556ce3-d3ed-4263-8ed8-95fd8c695f6a 61 fields · synced May 19, 2026
  • FDA UDI 2c116a96-9973-40a0-981a-1d25a7192a01 34 fields · synced May 30, 2026