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1X 23g Hfmn/Ahmd Hz Scissors, Cvd Shft

FDA UDI

Class I (US FDA UDI)

by Microsurgical Technology, Inc.

Identity

Trade Name
1X 23g Hfmn/Ahmd Hz Scissors, Cvd Shft FDA UDI
Generic Name
Intraocular scissors probe-tip, single-use FDA UDI
Model / Reference
DFH-1008-1 FDA UDI

Identifiers

Catalog Number
DFH-1008-1 FDA UDI
Primary DI / UDI-DI
00844685006113 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors probe-tip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intraocular scissors probe-tip, single-use

1X 23g Hfmn/Ahmd Hz Scissors, Cvd Shft by Microsurgical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors probe-tip, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e1b971d-c6d1-4fff-9b6f-911c5a60bc0f 33 fields · synced May 30, 2026