← Back to catalogue

LT ABO_Rh (D) Blood Grouping Card

FDA UDI

Class I (US FDA UDI)

by Zhuhai Longtime Biological Technology Co., Ltd

Identity

Trade Name
LT ABO_Rh (D) Blood Grouping Card FDA UDI
Generic Name
ABO/Rh multiple blood grouping IVD, kit, agglutination FDA UDI
Model / Reference
BGC-6 FDA UDI

Identifiers

Primary DI / UDI-DI
06974621793129 FDA UDI
FDA Product Code
KSY FDA UDI
GMDN Term
ABO/Rh multiple blood grouping IVD, kit, agglutination FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9185 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ABO/Rh multiple blood grouping IVD, kit, agglutination

LT ABO_Rh (D) Blood Grouping Card by Zhuhai Longtime Biological Technology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ABO/Rh multiple blood grouping IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c8df727c-6f1f-461e-9a34-e9c5dfb4c333 32 fields · synced Jun 8, 2026