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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
General-purpose surgical scissors, single-use FDA UDI
Device Name
METZENBAUM ADTEC SINGLE USE Dissecting Scissors, complete instrument, bipolar, curved to left, working length: 12 1/4", (310 mm), diam. 5 mm, blunt/blunt, rotatable, insulated, double action, sterile, disposable, package of 6 pieces FDA UDI
Model / Reference
PL700 FDA UDI
Description
METZENBAUM ADTEC SINGLE USE Dissecting Scissors, complete instrument, bipolar, curved to left, working length: 12 1/4", (310 mm), diam. 5 mm, blunt/blunt, rotatable, insulated, double action, sterile, disposable, package of 6 pieces FDA UDI

Identifiers

Catalog Number
PL700 FDA UDI
Primary DI / UDI-DI
04038653379668 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
General-purpose surgical scissors, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose surgical scissors, single-use

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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 445c50b8-9382-446f-8b05-5462d826a5f9 36 fields · synced May 31, 2026