← Back to catalogue

Adler Instrument Company

FDA UDI

Class I (US FDA UDI)

by Adler, Inc.

Identity

Trade Name
Adler Instrument Company FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Device Name
Lucae Ear Dress Fcps 5-1/2 FDA UDI
Model / Reference
48-0100 FDA UDI
Description
Lucae Ear Dress Fcps 5-1/2 FDA UDI

Identifiers

Primary DI / UDI-DI
00810123204830 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Surgical soft-tissue manipulation forceps, alligator, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, alligator, reusable.

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

Manufacturer
Adler, Inc.

Sources (1)

  • FDA UDI df175001-371e-484b-b656-33c4a0f902ea 34 fields · synced Jun 8, 2026