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Sponge Forceps

FDA UDI

Class I (US FDA UDI)

by Elmed Instruments(pvt)ltd.

Identity

Trade Name
SPONGE FORCEPS FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, single-use FDA UDI
Device Name
Intended Use: To hold gauze squares that will absorb excess fluids and blood. Packaging: Packaging shall be as per customer requirements e.g set of 25 or set of 50. FDA UDI
Model / Reference
SU-10-0095-24 FDA UDI
Description
Intended Use: To hold gauze squares that will absorb excess fluids and blood. Packaging: Packaging shall be as per customer requirements e.g set of 25 or set of 50. FDA UDI

Identifiers

Catalog Number
SU-10-0095-24 FDA UDI
Primary DI / UDI-DI
G165SU100095240 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Category: Dressing/utility forceps, scissors-like, single-use

Sponge Forceps by Elmed Instruments(pvt)ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, scissors-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Instruments(pvt)ltd.

Sources (1)

  • FDA UDI bbdcc1cb-2336-4433-85b7-ac64a4d48133 34 fields · synced Jun 8, 2026