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Removal Sleeve

FDA UDI

Class U (US FDA UDI)

by Surgentec Llc

Identity

Trade Name
Removal Sleeve FDA UDI
Generic Name
Spinal bone screw, bioabsorbable FDA UDI
Device Name
SR12- ION Facet Screw System FDA UDI
Model / Reference
SR12-6024 FDA UDI
Description
SR12- ION Facet Screw System FDA UDI

Identifiers

Primary DI / UDI-DI
00850040139143 FDA UDI
FDA Product Code
MRW FDA UDI
GMDN Term
Spinal bone screw, bioabsorbable FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, bioabsorbable

Removal Sleeve by Surgentec Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgentec Llc

Sources (1)

  • FDA UDI 36e52447-e064-4ec8-86ea-1b417ec08694 33 fields · synced May 30, 2026