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Adler Instrument Company

FDA UDI

Class I (US FDA UDI)

by Adler, Inc.

Identity

Trade Name
Adler Instrument Company FDA UDI
Generic Name
Blood component separator, manual FDA UDI
Device Name
Ferris Smith Tissue Forceps, 2 FDA UDI
Model / Reference
23-0290 FDA UDI
Description
Ferris Smith Tissue Forceps, 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00810123201839 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Blood component separator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Blood component separator, manual

Adler Instrument Company by Adler, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood component separator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adler, Inc.

Sources (1)

  • FDA UDI df7b0ffb-1ebe-46b1-bf78-b869d9e53ca1 34 fields · synced May 30, 2026