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Bur Sterilization Holder

FDA UDI

Class I (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
Bur Sterilization Holder FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Model / Reference
1600306 FDA UDI

Identifiers

Catalog Number
1600306-001 FDA UDI
Primary DI / UDI-DI
17630055505108 FDA UDI
FDA Product Code
MMO FDA UDI
GMDN Term
Surgical instrument interim-placement holder, 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: Surgical instrument interim-placement holder, reusable

Bur Sterilization Holder by Bien-Air Surgery SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Surgery SA

Sources (1)

  • FDA UDI b3c870ed-7d3c-4add-8e44-93f2bd7a34a3 33 fields · synced May 30, 2026