← Back to catalogue

Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
METZENBAUM (MINI) ADTEC BIPOLAR Dissecting Scissors, complete instrument, bipolar, curved to left, working length: 12 1/4", (310 mm), diam. 5 mm, (14 mm), blunt/blunt, rotatable, insulated, double action, consisting of PM437R, PM450R, PM973R, detachable, non-sterile, reusable FDA UDI
Model / Reference
PM407R FDA UDI
Description
METZENBAUM (MINI) ADTEC BIPOLAR Dissecting Scissors, complete instrument, bipolar, curved to left, working length: 12 1/4", (310 mm), diam. 5 mm, (14 mm), blunt/blunt, rotatable, insulated, double action, consisting of PM437R, PM450R, PM973R, detachable, non-sterile, reusable FDA UDI

Identifiers

Catalog Number
PM407R FDA UDI
Primary DI / UDI-DI
04038653305100 FDA UDI
FDA Product Code
HGI FDA UDI
GEI FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 FDA UDI
878.4400 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: General-purpose surgical scissors, reusable

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

Similar devices

Also classified as General-purpose surgical scissors, 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
Aesculap, Inc.

Sources (1)

  • FDA UDI 0b015c3e-91c8-4ca4-b496-b45bfe582097 36 fields · synced May 31, 2026