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Design Options®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Design Options® FDA UDI
Generic Name
Intrathecal anaesthesia set, medicated FDA UDI
Device Name
ALBANY MEDICAL CENTER, SSK FDA UDI
Model / Reference
560670 FDA UDI
Description
ALBANY MEDICAL CENTER, SSK FDA UDI

Identifiers

Catalog Number
560670 FDA UDI
Primary DI / UDI-DI
04046955595945 FDA UDI
FDA Product Code
OFU FDA UDI
GMDN Term
Intrathecal anaesthesia set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Intrathecal anaesthesia set, medicated

Design Options® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intrathecal anaesthesia set, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI 5bd72f7e-05f2-440d-8839-ef919a0c094b 37 fields · synced May 30, 2026