← Back to catalogue

Adler Instrument Company

FDA UDI

Class II (US FDA UDI)

by Adler, Inc.

Identity

Trade Name
Adler Instrument Company FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Device Name
Debakey Clamp 5 3/4 90 Degree FDA UDI
Model / Reference
42-0462 FDA UDI
Description
Debakey Clamp 5 3/4 90 Degree FDA UDI

Identifiers

Primary DI / UDI-DI
00810123205073 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

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, scissors-like, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, scissors-like, 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 122e3025-ca07-4361-a872-7a98706394b1 34 fields · synced May 31, 2026