Identity
- Trade Name
- MaxMoreSpine FDA UDI
- Generic Name
- Rigid endoscopic biopsy forceps, reusable FDA UDI
- Device Name
- Stenosis Kerrison, 250 mm/40° FDA UDI
- Model / Reference
- 1001-SK 002 FDA UDI
- Description
- Stenosis Kerrison, 250 mm/40° FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260200310958 FDA UDI
- FDA Product Code
- LRY FDA UDI
- GMDN Term
- Rigid endoscopic biopsy forceps, reusable 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rigid endoscopic biopsy forceps, reusable
MaxMoreSpine by Hoogland Spine Products, GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Rigid endoscopic biopsy forceps, reusable.
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- Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- ELMED — ELMED INCORPORATED · Class II
- UTERINE BIOSPY TRIANGULAR BASKET PUNCH — SONTEC INSTRUMENTS, INC. · Class I
- Biopsy forceps — Suzhou AcuVu Medical Technology Co., Ltd. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hoogland Spine Products, GmbH
Sources (1)
- FDA UDI 31072d6a-195d-4110-aa1a-06b37c117e8d 33 fields · synced May 30, 2026