Identity
- Trade Name
- MaxMoreSpine FDA UDI
- Generic Name
- Antimicrobial sensitivity disc dispenser IVD FDA UDI
- Device Name
- Detachable DiscDoctor forceps 260 mm / Ø 2.5 mm FDA UDI
- Model / Reference
- 1001-DF 001-D FDA UDI
- Description
- Detachable DiscDoctor forceps 260 mm / Ø 2.5 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260200313874 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Antimicrobial sensitivity disc dispenser IVD 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Antimicrobial sensitivity disc dispenser IVD
MaxMoreSpine by Hoogland Spine Products, GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Antimicrobial sensitivity disc dispenser IVD.
- BD BBL™ Sensi-Disc™ 12-Place Dispenser Cannister — BECTON DICKINSON AND COMPANY · Class II
- HardyDisk™ — HARDY DIAGNOSTICS · Class II
- HardyDisk™ — HARDY DIAGNOSTICS · Class II
- BD BBL™ Sensi-Disc™ Single Disc Dispenser — BECTON DICKINSON AND COMPANY · Class I
- BD BBL™ Sensi-Disc™ 6-Place Self-Tamping Dispenser — BECTON DICKINSON AND COMPANY · Class I
- BD BBL™ Sensi-Disc™ Single Disc Dispenser — BECTON DICKINSON AND COMPANY · Class I
- HardyDisk™ — HARDY DIAGNOSTICS · Class II
- BD BBL™ Sensi-Disc™ 8-Place Self-Tamping Dispenser — BECTON DICKINSON AND COMPANY · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hoogland Spine Products, GmbH
Sources (1)
- FDA UDI 2c4f003d-e9fb-4fc8-b2cf-7153bc878bc5 33 fields · synced May 30, 2026