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Ihc

FDA UDI

Class I (US FDA UDI)

by Slmp, LLC

Identity

Trade Name
IHC FDA UDI
Generic Name
pH-adjusted buffer solution IVD FDA UDI
Device Name
10X Tris-EDTA Retrieval Buffer, pH 9.0, 500 mL FDA UDI
Model / Reference
10X Tris-EDTA Retrieval Buffer, pH 9.0 FDA UDI
Description
10X Tris-EDTA Retrieval Buffer, pH 9.0, 500 mL FDA UDI

Identifiers

Catalog Number
ACR-003 FDA UDI
Primary DI / UDI-DI
00810170553585 FDA UDI
FDA Product Code
JCC FDA UDI
GMDN Term
pH-adjusted buffer solution IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: pH-adjusted buffer solution IVD

Ihc by Slmp, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as pH-adjusted buffer solution IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Slmp, LLC

Sources (1)

  • FDA UDI 033ad8f8-2b9c-4608-b0c3-16b1cecbd68e 34 fields · synced May 31, 2026