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Battery Assembly (2127 +2 more)

FDA UDI

Class II (US FDA UDI)

by Shenzhen Mindray Bio-Medical Electronics Co.

Identity

Trade Name
Battery Assembly(2127/Pack/FDA) FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Model / Reference
115-037256-00 FDA UDI

Identifiers

Primary DI / UDI-DI
06944904089690 FDA UDI
FDA Product Code
IYN FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack FDA UDI
Models / Variants
2127 FDA UDI
Pack FDA UDI
FDA FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1550 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Portable/mobile rechargeable battery pack

Battery Assembly (2127 +2 more) by Shenzhen Mindray Bio-Medical Electronics Co. — Class II — FDA UDI — listed in FDA GUDID — 3 models

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 204da5ce-b6d6-477a-8e38-71a59055ee83 33 fields · synced May 31, 2026