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Hey Groves Bone Holding Forceps, 310mm Length

FDA UDI

Class I (US FDA UDI)

by Platts & Nisbett Limited

Identity

Trade Name
Hey Groves Bone Holding Forceps, 310mm Length FDA UDI
Generic Name
Bone holding forceps FDA UDI
Model / Reference
PN0542 FDA UDI

Identifiers

Primary DI / UDI-DI
05056405503856 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bone holding forceps 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone holding forceps

Hey Groves Bone Holding Forceps, 310mm Length by Platts & Nisbett Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3f5aae62-6bd4-425d-b6c3-c126714edb84 32 fields · synced May 31, 2026