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B.braun

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
B.braun FDA UDI
Generic Name
General-purpose bowl, single-use FDA UDI
Device Name
Medicine Cup_60cc_Non-sterile_1150ea/cs FDA UDI
Model / Reference
15-0060AL FDA UDI
Description
Medicine Cup_60cc_Non-sterile_1150ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918199344 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
General-purpose bowl, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose bowl, single-use

B.braun by GRI Medical & Electronic Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose bowl, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1ee5f311-9a26-46e0-91ff-4a08bda3cc25 34 fields · synced Sep 18, 2026