← Back to catalogue

AccuFit Adhesive Housing, Oval, 30 pack

EUDAMEDFDA UDI

Class I (EU MDR)

Ref BE 6083

by Freudenberg Medical LLC

Identity

Trade Name
AccuFit Adhesive Housing, Oval, 30 pack EUDAMED
InHealth Technologies; Blom-Singer; Accufit FDA UDI
Generic Name
Tracheostomy base plate, single-use FDA UDI
Device Name
ACCUFIT EUDAMED
Model / Reference
BE 6083 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00848253003467 EUDAMED
00848253003498 FDA UDI
Basic UDI-DI
08482530ACCUFITF7 EUDAMED
FDA Product Code
BYD FDA UDI
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Tracheostomy base plate, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5375 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gas-sampling/monitoring respiratory tubing, single-use

AccuFit Adhesive Housing, Oval, 30 pack by Freudenberg Medical LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

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-000023823
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED fa2d90fa-8e4c-4c3b-bc75-b588f38d0c83 61 fields · synced Jun 19, 2026
  • FDA UDI 84308786-dcf6-4072-b881-e60e82315678 33 fields · synced May 30, 2026