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Tspace

EUDAMEDFDA UDI

Class I (EU MDR)

Ref FJ680R

by Aesculap AG

Identity

Trade Name
TSPACE EUDAMEDFDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
PROSPACE/TSPACE dissecting instrument EUDAMED
TSPACE Bone Curette, 45 °, (350 mm), width: 6,300 mm, non-sterile, reusable FDA UDI
Model / Reference
FJ680R EUDAMEDFDA UDI
Description
TSPACE Bone Curette, 45 °, (350 mm), width: 6,300 mm, non-sterile, reusable FDA UDI

Identifiers

Catalog Number
FJ680R FDA UDI
Primary DI / UDI-DI
04038653453313 EUDAMEDFDA UDI
Basic UDI-DI
4039239000000431ZT EUDAMED
FDA Product Code
FZS FDA UDI
EMDN Code
L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany 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

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: Bone curette, reusable

Tspace by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED 719625a3-d8ab-4957-b2eb-589905bbd8c6 61 fields · synced Jun 19, 2026
  • FDA UDI 8a4ae1de-6835-4493-8ab4-313897e4f03f 35 fields · synced May 30, 2026