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Maskenkruemmer

FDA UDI

Class I (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
MASKENKRUEMMER FDA UDI
Generic Name
Straight/elbow breathing circuit connector, reusable FDA UDI
Model / Reference
M25649 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675235071 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Straight/elbow breathing circuit connector, reusable

Maskenkruemmer by Drägerwerk AG & Co. KGaA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Straight/elbow breathing circuit connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drägerwerk AG & Co. KGaA

Sources (1)

  • FDA UDI 7261b001-7256-4179-a65c-f19c4f2635fc 33 fields · synced Jun 8, 2026