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Potts-Smith Tissue Forceps

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Potts-Smith Tissue Forceps FDA UDI
Generic Name
Uterine tenaculum FDA UDI
Device Name
Potts-Smith Tissue Forceps- 1x2 Teeth- Length: 208 mm FDA UDI
Model / Reference
61872 FDA UDI
Description
Potts-Smith Tissue Forceps- 1x2 Teeth- Length: 208 mm FDA UDI

Identifiers

Primary DI / UDI-DI
00888937019094 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Uterine tenaculum 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

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

Yes

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

Dimensions & Sizes

Size
Length — 208 Millimeter FDA UDI

Category: Uterine tenaculum

Potts-Smith Tissue Forceps by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uterine tenaculum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20818e0d-00fd-400d-a4ae-44eb802743d4 34 fields · synced Jun 9, 2026