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Immucor Precise TypeTM Human Erythrocyte Antigen Molecular BeadChip Test Plate

FDA UDI

Class III (US FDA UDI)

by Bioarray Solutions Ltd

Identity

Trade Name
Immucor Precise TypeTM Human Erythrocyte Antigen Molecular BeadChip Test Plate FDA UDI
Generic Name
Multiple blood group genotyping IVD, nucleic acid technique (NAT) FDA UDI
Model / Reference
800-20202-96 FDA UDI

Identifiers

Catalog Number
800-20202-96 FDA UDI
Primary DI / UDI-DI
10888234102618 FDA UDI
FDA Product Code
PEP FDA UDI
GMDN Term
Multiple blood group genotyping IVD, nucleic acid technique (NAT) FDA UDI

Classification

Device Class
Class III 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple blood group genotyping IVD, nucleic acid technique (NAT)

Immucor Precise TypeTM Human Erythrocyte Antigen Molecular BeadChip Test Plate by Bioarray Solutions Ltd — Class III — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Multiple blood group genotyping IVD, nucleic acid technique (NAT).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 92df75a0-2723-492a-a113-3684dacddb5d 35 fields · synced Jun 8, 2026