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OSSEOSTAP Sterilization Tray

FDA UDIEUDAMED

Class I (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
OSSEOSTAP Sterilization Tray FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Model / Reference
1600669 FDA UDI

Identifiers

Catalog Number
1600669-001 FDA UDI
Primary DI / UDI-DI
07630055505620 FDA UDI
FDA Product Code
MMO FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

Category: Device sterilization/disinfection container, reusable

OSSEOSTAP Sterilization Tray by Bien-Air Surgery SA — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Surgery SA

Sources (2)

  • FDA UDI 93df83a4-1691-4bd4-885b-411135be1428 33 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026