← Back to catalogue

Tongue blade

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 40-509-17

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Tongue blade FDA UDI
Generic Name
Tongue depressor, surgical FDA UDI
Device Name
Spatulas EUDAMED
s-shape 17 cm FDA UDI
Model / Reference
40-509-17 EUDAMEDFDA UDI
Description
s-shape 17 cm FDA UDI

Identifiers

Catalog Number
40-509-17 FDA UDI
Primary DI / UDI-DI
04250676734006 EUDAMEDFDA UDI
Basic UDI-DI
425038185G0501S2 EUDAMED
Direct Marketing DI
04250676734006 EUDAMED
FDA Product Code
KBL FDA UDI
EMDN Code
L14010205 OROPHARYNGAL SURGERY DEPRESSORS, REUSABLE EUDAMED
GMDN Term
Tongue depressor, surgical FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
874.4420 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tongue depressor, surgical

Tongue blade by Spiggle & Theis Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tongue depressor, surgical.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 32a3213f-5e86-4530-8fb4-2afb50ab39f8 35 fields · synced Oct 8, 2026
  • EUDAMED e6194051-2157-4ed3-aeaa-c6211575f0af 61 fields · synced Oct 8, 2026