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ErgoStar AC 95

FDA UDIEUDAMED

Class I (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
ErgoStar AC 95 FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Model / Reference
MP01895 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675042686 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Straight/elbow breathing circuit connector, single-use

ErgoStar AC 95 by Drägerwerk AG & Co. KGaA — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Straight/elbow breathing circuit connector, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI bed2430f-4dde-4a7f-9408-5bb9802da9e7 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026