← Back to catalogue

Healing/Closure Screw

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 036.2204S

by Institut Straumann AG

Identity

Trade Name
Straumann TLX Implant System FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Healing/Closure Screw EUDAMED
WT Healing Cap, Ø7.2mm, H4.5mm, Ti FDA UDI
Model / Reference
036.2204S EUDAMED
Healing Components FDA UDI
Description
WT Healing Cap, Ø7.2mm, H4.5mm, Ti FDA UDI

Identifiers

Catalog Number
036.2204S FDA UDI
Primary DI / UDI-DI
07630031746436 EUDAMEDFDA UDI
Basic UDI-DI
0763003170065QW EUDAMED
510(k) Number
K200586 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Height — 4.5 Millimeter FDA UDI
Outer Diameter — 7.2 Millimeter FDA UDI

Healing/Closure Screw by Institut Straumann AG — Class IIb — 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
CH-MF-000009933
Authorised Representative
Etkon GmbH DE-AR-000009335

Sources (2)

  • EUDAMED 6108364c-5852-4aab-b2ca-a81a6c9aa29c 61 fields · synced Jun 9, 2026
  • FDA UDI 2d8e5d40-60bf-4fc5-aa63-102bed0d0250 38 fields · synced May 30, 2026